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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Span. J. Soil Sci.</journal-id>
<journal-title>Spanish Journal of Soil Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Span. J. Soil Sci.</abbrev-journal-title>
<issn pub-type="epub">2253-6574</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">11302</article-id>
<article-id pub-id-type="doi">10.3389/sjss.2023.11302</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Science archive</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Genomic Assessment of <italic>Enterobacter mori</italic> AYS9: A Potential Plant Growth-Promoting Drought-Resistant Rhizobacteria</article-title>
<alt-title alt-title-type="left-running-head">Fadiji et al.</alt-title>
<alt-title alt-title-type="right-running-head">Genomic Assessment of <italic>Enterobacter mori</italic>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Fadiji</surname>
<given-names>Ayomide Emmanuel</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/960825/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ayangbenro</surname>
<given-names>Ayansina Segun</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/185707/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Babalola</surname>
<given-names>Olubukola Oluranti</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/93752/overview"/>
</contrib>
</contrib-group>
<aff>
<institution>Food Security and Safety Focus Area</institution>, <institution>Faculty of Natural and Agricultural Sciences</institution>, <institution>North-West University</institution>, <addr-line>Mmabatho</addr-line>, <country>South Africa</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/89410/overview">Avelino N&#xfa;&#xf1;ez-Delgado</ext-link>, University of Santiago de Compostela, Spain</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Olubukola Oluranti Babalola, <email>olubukola.babalola@nwu.ac.za</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>08</day>
<month>06</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>13</volume>
<elocation-id>11302</elocation-id>
<history>
<date date-type="received">
<day>23</day>
<month>02</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>31</day>
<month>05</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Fadiji, Ayangbenro and Babalola.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Fadiji, Ayangbenro and Babalola</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Drought stress poses a serious danger to agricultural production. Recent studies have revealed that most of the chemical methods used in the mitigation of its effects on plant production pose a serious threat to humans and the environment. Therefore, the demand for ecologically friendly solutions to ensure the security of the world&#x2019;s food supply has increased as a result. Plant growth-promoting rhizobacteria (PGPR) treatment may be advantageous in this situation. <italic>Enterobacter mori</italic> is a promising rhizobacteria in this regard. However, information on the genome analysis of <italic>E. mori</italic> linked to the rhizosphere soil of the sorghum plant has not been extensively studied. In this study, we present a genomic lens into functional attributes of <italic>E. mori</italic> AYS9 isolated from sorghum plants, as well as assess its drought tolerance and plant growth-promoting potentials. Our results showed the drought tolerance and plant growth-promoting potentials of the AYS9. Whole genome sequencing (WGS) results revealed that the genome yielded 4,852,175&#xa0;bp sequence reads, an average read length of 151&#xa0;bp, 1,845,357&#xa0;bp genome size, 67 tRNAs, 3 rRNAs, and a G &#x2b; C content of 55.5%. The functional genes identified in the genome were linked to processes including phosphate solubilization, iron transport, hormone regulation, nitrogen fixation, and resistance to oxidative and osmotic stress. Also, secondary metabolites supporting bacterial biocontrol properties against phytopathogens, and abiotic stress such as aerobactin-type non-ribosomal peptide siderophore, Stewartan-type ladderane, and Colicin type NRPS were discovered in the AYS9 genome. Our findings however establish that the intricate metabolic pathways mediated by the projected new genes in the bacterial genome may offer a genetic foundation for future understanding of rhizosphere biology and the diverse roles that these genes play in plant development and health.</p>
</abstract>
<kwd-group>
<kwd>sustainable agriculture</kwd>
<kwd>abiotic stress</kwd>
<kwd>plant health improvement</kwd>
<kwd>rhizobacteria</kwd>
<kwd>crop productivity</kwd>
</kwd-group>
<contract-sponsor id="cn001">National Research Foundation<named-content content-type="fundref-id">10.13039/501100001321</named-content>
</contract-sponsor>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>A major abiotic stress that poses a danger to global agricultural productivity is drought (<xref ref-type="bibr" rid="B21">Fadiji et al., 2022b</xref>; <xref ref-type="bibr" rid="B22">Fadiji et al., 2022c</xref>). Lack of access to fresh water to satisfy the needs of humans and the environment causes and sustains drought, which is a natural phenomenon (<xref ref-type="bibr" rid="B7">Balint et al., 2013</xref>; <xref ref-type="bibr" rid="B55">Ojuederie et al., 2019</xref>). Since drought is frequently not localised to a certain time or place, monitoring it may be challenging. Lack of water causes serious socioeconomic problems, and crop loss, and is fatal to plants (<xref ref-type="bibr" rid="B62">Salehi-Lisar and Bakhshayeshan-Agdam, 2016</xref>; <xref ref-type="bibr" rid="B1">Ahluwalia et al., 2021</xref>). <xref ref-type="bibr" rid="B61">Ramakrishna et al. (2019)</xref> and <xref ref-type="bibr" rid="B21">Fadiji et al. (2022b)</xref> reported that roughly half of the arable land will likely be severely drought-restricted in terms of plant growth by 2052. According to (<xref ref-type="bibr" rid="B40">Mach et al., 2019</xref>), drought stress has lowered grain yields by up to 10% over the past 40&#xa0;years and is expected to have an impact on the output above 50% of most fertile land by the year 2050 (<xref ref-type="bibr" rid="B78">Vinocur and Altman, 2005</xref>; <xref ref-type="bibr" rid="B31">Jochum et al., 2019</xref>). Research has concentrated on enhancing germplasm and creating techniques for crop management to boost water usage efficiency in order to meet this worldwide challenge in agriculture (<xref ref-type="bibr" rid="B51">Ngumbi and Kloepper, 2016</xref>). Due to technological advancements in microbiomics and next-generation sequencing, however, the focus has recently shifted to the use of beneficial microbes that mediate tolerance to drought and increase plant water usage efficiency (<xref ref-type="bibr" rid="B16">Dimkpa et al., 2009</xref>; <xref ref-type="bibr" rid="B51">Ngumbi and Kloepper, 2016</xref>; <xref ref-type="bibr" rid="B79">Vurukonda et al., 2016</xref>).</p>
<p>A sustainable biological strategy to address agricultural production&#x2019;s water shortage is the use of plant growth-promoting rhizobacteria (PGPR). Intimate and free-living relationships with host plants are quickly established by PGPR in the root rhizosphere. Through a number of processes, these interactions frequently result in an improvement in agricultural yield and the reduction of abiotic and biotic stressors (<xref ref-type="bibr" rid="B79">Vurukonda et al., 2016</xref>; <xref ref-type="bibr" rid="B8">Barnawal et al., 2017</xref>; <xref ref-type="bibr" rid="B23">Forni et al., 2017</xref>). Having been reported as plant disease suppressors, biofertilizers, abiotic stress relievers, and soil toxin removers, PGPR may be extremely important (<xref ref-type="bibr" rid="B50">Naveed et al., 2014</xref>; <xref ref-type="bibr" rid="B77">Timmusk et al., 2014</xref>). Changes in the structure of the osmoregulation, host root system, management of oxidative stress through the biosynthesis and metabolism of phytohormones or the production of antioxidants for scavenging reactive oxygen species (ROS), the production of large chain exopolysaccharide (EPS), which may act as a humectant, and transcriptional control of the genes responsible for host stress response are some of the mechanisms connected to PGPR-derived drought tolerance (<xref ref-type="bibr" rid="B51">Ngumbi and Kloepper, 2016</xref>; <xref ref-type="bibr" rid="B23">Forni et al., 2017</xref>; <xref ref-type="bibr" rid="B20">Fadiji et al., 2022a</xref>; <xref ref-type="bibr" rid="B22">Fadiji et al., 2022c</xref>).</p>
<p>The genus <italic>Enterobacter</italic> has a total of 23 known species (<ext-link ext-link-type="uri" xlink:href="http://www.bacterio.cict.fr/e/enterobacter.html">http://www.bacterio.cict.fr/e/enterobacter.html</ext-link>). Both as pathogenic and beneficial species, <italic>Enterobacter</italic> species have been implicated in plant diseases and human opportunistic pathogens (<xref ref-type="bibr" rid="B53">Nishijima et al., 2007</xref>), as well as essential genetic engineering and plant growth-promoting bacteria (<xref ref-type="bibr" rid="B52">Nie et al., 2002</xref>). Others also play vital roles in biocontrol (<xref ref-type="bibr" rid="B85">Zhu et al., 2011</xref>). However, only a limited number of <italic>Enterobacter</italic> species have been identified in plants and soils, although they play numerous functions in plant metabolism and physiology (<xref ref-type="bibr" rid="B85">Zhu et al., 2011</xref>; <xref ref-type="bibr" rid="B31">Jochum et al., 2019</xref>). For instance, due to their capacity to produce osmoprotective genes and substances, <italic>E. mori</italic> strains have been widely isolated from the rhizosphere soil of many plants and have been actively involved in the reduction of drought stress in plants. Hence, it may be concluded that <italic>E. mori</italic> has a potential future in agricultural sustainability.</p>
<p>The identification of key genes in the genome of <italic>Enterobacter</italic> species might greatly improve these bacteria&#x2019;s roles in the development of root-bacterial, soil-bacterial, and soil-root interactions for better plant stress response mechanisms (<xref ref-type="bibr" rid="B80">Vurukonda et al., 2018</xref>). The lifestyle and operations of the bacteria in the host plants can be impacted by these genes. For instance, the discovery of genes known in the development of biofilm chemotaxis can support plant defense systems and colonization of the root. Based on these functional presumptions, <italic>E. mori</italic> can be a viable bioagent in the formulation of biostimulants and bioinoculants against drought and for better agricultural yield. In this study, we present a genomic lens into the functional attributes of <italic>E. mori</italic> AYS9, as well as assess its drought tolerance and plant growth-promoting potentials. As far as we know, this is one of the foremost reports on the WGS of <italic>E. mori</italic> AYS9 isolated from the rhizosphere of sorghum plants in Southern Africa. Furthermore, this study assessed the plant growth-promoting activities, presence of functional genes and secondary metabolites of the strain.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>Materials and Methods</title>
<sec id="s2-1">
<title>Sampling and Isolation of Rhizobacteria <italic>Enterobacter mori</italic> AYS9</title>
<p>The rhizobacterium was isolated from 10&#xa0;g of rhizosphere soil from healthy sorghum plants cultivated in the research farm of the North-West University, South Africa (250 47&#x2032;25.24056&#x2033; S 250 37&#x2032;30 8.17464&#x2033; E). The isolation and characterization of the rhizobacterial isolate were carried out using the method of <xref ref-type="bibr" rid="B69">Sha&#x2019;arani et al. (2021)</xref>. A pure rhizobacterium was isolated from 10&#xa0;g soil tightly adhering to the root of the sorghum through serial dilution and subsequent culturing on Luria&#x2013;Bertani (LB) agar plates using the method of <xref ref-type="bibr" rid="B43">Majeed et al. (2015)</xref>. After a series of subculturing, the identified single colonies were characterized using morphological and biochemical tests. The distinct colony was further selected and purified, which was then maintained on a sterile nutrient agar slant for further analyses.</p>
</sec>
<sec id="s2-2">
<title>Morphological, Microscopic Appearance, and Biochemical Characterization of <italic>Enterobacter mori</italic> AYS9</title>
<p>The pure culture of <italic>E. mori</italic> AYS9 was plated on Nutrient agar and incubated at 28&#xb0;C for 24&#xa0;h after which the morphological characteristics of the isolate were examined. The colonies&#x2019; morphology, which includes shape, size, pigmentation, and color was properly documented after incubation. Furthermore, the biochemical characterization such as Gram staining, including oxidase, nitrate reduction, Voges Proskauer, catalase, indole, citrate, and starch hydrolysis test by using the standardized method as reported by <xref ref-type="bibr" rid="B15">Clarke and Cowan (1952)</xref> and <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref>. While carbohydrate utilization potentials of the AYS9 were carried out using carbon sources such as galactose, maltose, xylose, lactose, fructose, glucose and sucrose (<xref ref-type="bibr" rid="B66">Sati and Bisht, 2006</xref>).</p>
</sec>
<sec id="s2-3">
<title>Screening of the <italic>Enterobacter mori</italic> AYS9 for Drought Tolerance Under Increasing Concentrations of Polyethylene Glycol (PEG6000)</title>
<p>Assessment of the osmotic tolerance of <italic>E. mori</italic> AYS9 was carried out by documenting their growth within the nutrient-broth medium adjusted with varying PEG6000 concentrations (0%&#x2013;30%). The cultures were then incubated for 48&#xa0;h at 28&#xb0;C under shaking at 200&#xa0;rpm at the same time (<xref ref-type="bibr" rid="B64">Sandhya et al., 2009</xref>). Estimation of the bacterial growth was done by properly recording the cultures&#x2019; optical density of the medium at various concentrations of PEG 6000 using Merck&#x2019;s UV spectrophotometer at 600&#xa0;nm.</p>
</sec>
<sec id="s2-4">
<title>Screening of <italic>Enterobacter mori</italic> AYS9 for PGP Traits</title>
<p>The standardized methods, as described by <xref ref-type="bibr" rid="B13">Cappuccino and Sherman (1992)</xref>, as well as <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref>, were utilized in the testing of <italic>E. mori</italic> AYS9 for NH<sub>3</sub> production in peptone water. The test for phosphate solubilization was done employing a modified procedure as described by <xref ref-type="bibr" rid="B71">Shakeela et al. (2017)</xref>. The procedures of <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref>, in addition to those of <xref ref-type="bibr" rid="B44">Masciarelli et al. (2014)</xref>, were employed to test isolated bacteria for siderophore production. The nutrient broth culture of the isolate was used to inoculate tri-calcium phosphate-supplemented Pikovskaya&#x2019;s agar. The emergence of yellow coloration around the bacterial inoculation spot, thus, implied a positive result. The nitrogen fixation characteristics of the endophytic bacteria were determined according to <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref> in Jensen&#x2019;s medium. Bacterial growth in the medium indicated the nitrogen-fixing potential.</p>
<p>Furthermore, modified procedures of <xref ref-type="bibr" rid="B38">Loper and Schroth (1986)</xref> and <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref> were used to determine indole-3-acetic acid (IAA) qualitatively at varying concentrations of tryptophan of 0, 100, and 200&#xa0;mg within the nutrient broth. The IAA production was signaled by the emergence of pink coloration. Screening of isolate for hydrogen cyanide production (HCN) was also carried out using the procedure described by <xref ref-type="bibr" rid="B2">Ahmad et al. (2008)</xref> with slight modifications. The HCN production was indicated by the emergence of orange-to-red coloration. Also, the potential of the isolate to produce 1-aminocyclopropane-1-carboxylate deaminase (ACCd) enzyme was examined on account of the capability to utilize ACC as the only source of nitrogen within the minimal medium (<xref ref-type="bibr" rid="B17">Duan et al., 2009</xref>). Bacterial growth on the supplemented ammonium sulphate medium indicated ACCd activity.</p>
</sec>
<sec id="s2-5">
<title>Whole-Genome Sequencing (WGS) and Analysis of <italic>Enterobacter mori</italic> Strain AYS9</title>
<p>The extraction of the DNA of <italic>E. mori</italic> strain AYS9 was carried out using the Quick-DNA&#x2122; Miniprep Kit specific for bacteria and fungi (Zymo Research, United States), using the method stipulated by the manufacturer. DNA quality checks were carried out using a NanoDrop spectrophotometry (Thermo Fischer Scientific, United States). The molecular identification and analysis of the stain AYS9 based on 16S rDNA sequence data was carried out using the method of <xref ref-type="bibr" rid="B43">Majeed et al. (2015)</xref>. The genome sequencing of the strain AYS9 was performed at the Novogene Company Limited, Singapore.</p>
<p>The WGS of the rhizobacteria strain AYS9 was carried out using the employing of the standard Illumina platform. Furthermore, fragmentation of the genomic DNA of the bacteria was done employing the NEB Ultra II FS kit enzymatic technique. AMPure XP beads were used to assess the resulting fragments of the DNA based on size range (200&#x2013;650&#xa0;bp). Also, end-repairing of the DNA was achieved through fragmentation, and the fragment was ligated to Illumina-specifc adapter sequences. Consequently, the sample indexing and selection depending on the size in the second step were carried out. The 4&#xa0;nM quantity dilution of the standard dilution concentration of the samples was achieved using the fluorometric method. Consequently, sequencing was performed using the pair-end Illumina library and was loaded into the NovaSeq 6000 (2 &#xd7; 150&#xa0;bp) instrument for cluster generation and sequencing (300 cycles).</p>
<p>The WGS analysis of the sequence in FASTQ file format was uploaded to the Department of Energy Systems Biology Knowledgebase (KBase) (<xref ref-type="bibr" rid="B4">Arkin et al., 2018</xref>). The assessment of the quality of each sequence reads was performed with FastQC tool (version 0.11.5) (<xref ref-type="bibr" rid="B3">Andrews, 2010</xref>), while the removal of low-quality bases and sequence adaptor was performed using trimmomatics (version 0.36) (<xref ref-type="bibr" rid="B11">Bolger et al., 2014</xref>). Also, sequence reads were assembled by SPAdes (version 3.13.0) (<xref ref-type="bibr" rid="B54">Nurk et al., 2013</xref>). Taxonomic annotation was carried out using the GTDB-Tk - v1.7.0 (<xref ref-type="bibr" rid="B14">Chaumeil et al., 2020</xref>), while functions annotation was carried out using Rapid Annotations using Subsystems Technology toolkit (RASTtk) (version 1.073) (<xref ref-type="bibr" rid="B5">Aziz et al., 2008</xref>) and SEED online server (<xref ref-type="bibr" rid="B57">Overbeek et al., 2014</xref>) to group the functions and distribution of the predicted genes. The prediction of functional protein-coding genes was performed using the genomic protein data after processing the genome on the National Center for Biotechnology Information (NCBI) database (<xref ref-type="bibr" rid="B36">Li et al., 2021</xref>). All analyses in this study were done using default parameters except otherwise stated. Determination of secondary metabolites in the genome was carried out using antiSMASH (version 6.0.0) (<xref ref-type="bibr" rid="B84">Weber et al., 2015</xref>). The circular visualization of the genome with the important genomic feature was plotted using Circular Genome Viewer (CGview) (<xref ref-type="bibr" rid="B4">Arkin et al., 2018</xref>), while the phylogeny analysis was performed using MrBayes (<xref ref-type="bibr" rid="B26">Huelsenbeck and Ronquist, 2001</xref>). The antiSMASH version 6.0 (<xref ref-type="bibr" rid="B9">Blin et al., 2021</xref>) was used for the detection of important metabolites and their biosynthetic gene clusters.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec id="s3-1">
<title>Biochemical, Cultural Features and Drought Tolerance Assay</title>
<p>The cultural, and biochemical characterization alongside plant growth promoting (PGP) features of <italic>Enterobacter mori</italic> AYS9 from the rhizosphere of the sorghum plant was presented in <xref ref-type="table" rid="T1">Table 1</xref>. The results showed that AYS9 is Gram-negative, rod-shaped, creamy in colour and catalase positive. Furthermore, strain AYS9 utilizes all the sugars tests carried out and grows optimally between the pH range of 4&#x2013;10 and temperatures of 20&#xb0;C&#x2013;30&#xb0;C. The plant growth-promoting assay carried out on the strain showed that the strain AYS9 tested positive for all the PGP traits, such as the production of ammonia, phosphate, siderophore, indole-3-acetic acid (IAA), 1-aminocyclopropane-1-carboxylate deaminase (ACCd) as well as nitrogen fixation. But tested negative for hydrogen cyanide production (<xref ref-type="table" rid="T1">Table 1</xref>). A drought tolerance assay carried out on the strain showed that the strain exhibited increased tolerance to Polyethylene glycol (PEG6000) even to a 30% concentration (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Cultural, biochemical and plant growth-promoting test of <italic>Enterobacter mori</italic> AYS9.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th colspan="2" align="left">Cultural and biochemical assay</th>
<th colspan="2" align="center">Plant growth-promoting qualitative tests</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Characteristics</td>
<td align="left">Result</td>
<td align="left">PGP traits</td>
<td align="center">Results</td>
</tr>
<tr>
<td align="left">Shape</td>
<td align="left">Rods</td>
<td align="left">Ammonia production</td>
<td align="left">&#x2b;&#x2b;</td>
</tr>
<tr>
<td align="left">Gram reaction</td>
<td align="left">Gram-negative</td>
<td align="left">Phosphate solubilization</td>
<td align="left">&#x2b;&#x2b;</td>
</tr>
<tr>
<td align="left">Color</td>
<td align="left">Cream</td>
<td align="left">Siderophore</td>
<td align="left">&#x2b;</td>
</tr>
<tr>
<td align="left">Surface texture</td>
<td align="left">Smooth shiny</td>
<td align="left">Nitrogen fixation</td>
<td align="left">&#x2b;</td>
</tr>
<tr>
<td align="left">Citrate</td>
<td align="left">&#x2b;</td>
<td align="left">IAA</td>
<td align="left">&#x2b;</td>
</tr>
<tr>
<td align="left">Catalase</td>
<td align="left">&#x2b;</td>
<td align="left">HCN</td>
<td align="left">&#x2212;</td>
</tr>
<tr>
<td align="left">Nitrate</td>
<td align="left">&#x2b;</td>
<td align="left">ACCd</td>
<td align="left">&#x2b;&#x2b;</td>
</tr>
<tr>
<td align="left">Maltose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Oxidase</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Casein hydrolysis</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Fructose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Glucose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Sucrose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Trehalose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Turanose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Galactose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Xylose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Mannitol</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Arabinose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Raffinose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
<tr>
<td align="left">Maltose</td>
<td align="left">&#x2b;</td>
<td align="left"/>
<td align="left"/>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Response of <italic>Enterobacter mori</italic> AYS9 to drought stress amended with various concentrations of PEG-6000.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Treatment</th>
<th align="center">O.D at 600&#xa0;nm</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">0%</td>
<td align="center">1.38 &#xb1; 0.06</td>
</tr>
<tr>
<td align="left">5%</td>
<td align="center">1.04 &#xb1; 0.01</td>
</tr>
<tr>
<td align="left">10%</td>
<td align="center">0.88 &#xb1; 0.03</td>
</tr>
<tr>
<td align="left">15%</td>
<td align="center">0.74 &#xb1; 0.02</td>
</tr>
<tr>
<td align="left">20%</td>
<td align="center">0.76 &#xb1; 0.01</td>
</tr>
<tr>
<td align="left">25%</td>
<td align="center">0.89 &#xb1; 0.02</td>
</tr>
<tr>
<td align="left">30%</td>
<td align="center">0.96 &#xb1; 0.03</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Values are represented as the mean of 3 replicates (<italic>n</italic> &#x3d; 3) &#xb1;SE.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3-2">
<title>WGS Information of the Rhizobacterium <italic>Enterobacter mori</italic> AYS9</title>
<p>The WGS assessment of <italic>E. mori</italic> AYS9 showed 7,301,524&#xa0;bp sequence read count, genome size is 4,852,175&#xa0;bp, and a G &#x2b; C content of 55.5% as seen in <xref ref-type="table" rid="T3">Table 3</xref>. The read length average was 151&#xa0;bp, while <italic>L</italic>
<sub>50</sub> and <italic>N</italic>
<sub>50</sub> were 2 and 632,440&#xa0;bp, respectively while the number of contigs is 34. Furthermore, the genome analysis showcased 4,546 coding sequences, 67 tRNA and 3 rRNA. The circular genome visualization of <italic>E. mori</italic> strain AYS9 is shown in <xref ref-type="fig" rid="F1">Figure 1</xref>. The statistics of the subsystem revealed 27 subsystem features of the coding protein into functional groups based on the annotated genome grouping by the SEED subsystem in RAST online server. The functional groups of 4,546 protein-coding genes (PCG) were assessed using the RAST and KEGG databases. The 1,732 genes annotated using SEED were classified into cellular components, molecular functions, and biological processes. The six functional groups were found to be prominent these groups are stress response (95 genes), Protein Metabolism (220 genes), carbohydrates (329 genes), Amino Acids and Derivatives (350 genes), respiration (99 genes), cofactor vitamins, prosthetic groups, and pigments (157 genes) (<xref ref-type="fig" rid="F2">Figure 2</xref>).</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>General characteristics of the genome and annotation details of <italic>Enterobacter mori</italic> AYS9.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Treatment</th>
<th align="center">
<italic>Enterobacter mori</italic> stain AYS9</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Domain</td>
<td align="left">Bacteria</td>
</tr>
<tr>
<td align="left">Taxonomy</td>
<td align="left">Proteobacteria, Gammaproteobacteria; Enterobacterales, Enterobacteriaceae, <italic>Enterobacter</italic>
</td>
</tr>
<tr>
<td align="left">Size(bp)</td>
<td align="left">4,852,175</td>
</tr>
<tr>
<td align="left">G &#x2b; C content (%)</td>
<td align="left">55.5</td>
</tr>
<tr>
<td align="left">
<italic>N</italic>50</td>
<td align="left">632,440</td>
</tr>
<tr>
<td align="left">
<italic>L</italic>50</td>
<td align="left">2</td>
</tr>
<tr>
<td align="left">Number of contigs (with PEGs)</td>
<td align="left">34</td>
</tr>
<tr>
<td align="left">Number of subsystems</td>
<td align="left">372</td>
</tr>
<tr>
<td align="left">Number of coding sequences</td>
<td align="left">4,446</td>
</tr>
<tr>
<td align="left">Number of RNAs</td>
<td align="left">76</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Circular genome visualization of whole-genome <italic>Enterobacter mori</italic> AYS9.</p>
</caption>
<graphic xlink:href="sjss-13-11302-g001.tif"/>
</fig>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Major PCG of <italic>Enterobacter mori</italic> strain AYS9 annotated in the RAST and SEED Viewer annotation online server. The green/blue bar on the left shows the coverage of the subsystemin percentage. The blue bar shows the proteins percentage present.</p>
</caption>
<graphic xlink:href="sjss-13-11302-g002.tif"/>
</fig>
</sec>
<sec id="s3-3">
<title>Functional Genes Annotation Information of <italic>Enterobacter mori</italic> AYS9</title>
<p>Notable metabolic genes were identified in the AYS9 genome (<xref ref-type="table" rid="T4">Tables 4</xref>&#x2013;<xref ref-type="table" rid="T6">6</xref>). Notable genes involved in phosphate solubilization and pathways, such as phosphate assimilation and phosphate transport, are presented in <xref ref-type="table" rid="T4">Table 4</xref>. The genes, such as <italic>fbpC</italic> and <italic>feoA</italic>, coding for iron transport in the Iron (III) transport and Iron (II) transport were detected in strain AYS9 (<xref ref-type="table" rid="T5">Table 5</xref>). Genes, such as <italic>trpA</italic>, <italic>trpB miaA</italic>, <italic>miaB speA</italic>, <italic>speB</italic>, <italic>speD</italic>, <italic>speE speG</italic>, <italic>nirB</italic>, <italic>nirD</italic>, <italic>amtB</italic>, <italic>ureC</italic>, <italic>ureG</italic>, <italic>ureF</italic>, <italic>ureE</italic> coding for iron transport, modulation and nitrogen metabolism in the L-tryptophan production, CK biosynthesis, putrescine biosynthesis, spermidine biosynthesis, N1- and N8-acetylspermidine formation, dissimilatory nitrate reduction, ammonia transport, urea degradation and transport respectively are similarly presented in <xref ref-type="table" rid="T5">Table 5</xref>. Other important genes involved in the mitigation of osmotic and oxidative pathways, such as glycine betaine biosynthesis, proline biosynthesis, glutamate biosynthesis, glycine betaine/proline transport system, glutamate transport, degradation of hydrogen peroxide and degradation of hydrogen peroxide and organic hydroperoxides (<xref ref-type="table" rid="T6">Table 6</xref>).</p>
<table-wrap id="T4" position="float">
<label>TABLE 4</label>
<caption>
<p>Notable genes identified in phosphate transport and solubilization.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Genes</th>
<th align="center">Locus Tag</th>
<th align="center">Product</th>
<th align="center">Pathways</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">
<italic>ppa</italic>
</td>
<td align="center">N4Q52_12890</td>
<td align="left">Inorganic pyrophosphatase</td>
<td rowspan="6" align="left">Phosphate assimilation</td>
</tr>
<tr>
<td align="left">
<italic>pgl</italic>
</td>
<td align="center">N4Q52_18515</td>
<td align="left">6- phosphogluconolactonase</td>
</tr>
<tr>
<td align="left">ppx</td>
<td align="center">N4Q52_08230</td>
<td align="left">Exopolyphosphatase</td>
</tr>
<tr>
<td align="left">
<italic>pst</italic>C</td>
<td align="center">N4Q52_08250</td>
<td align="left">P (ABC)T permease subunit <italic>Pst</italic>C</td>
</tr>
<tr>
<td align="left">
<italic>pho</italic>U</td>
<td align="center">N4Q52_18765</td>
<td align="left">Phosphate signaling complex protein <italic>Pho</italic>U</td>
</tr>
<tr>
<td align="left">
<italic>pho</italic>A</td>
<td align="center">N4Q52_15190</td>
<td align="left">Alkaline phosphatase</td>
</tr>
<tr>
<td align="left">
<italic>pst</italic>A</td>
<td align="center">N4Q52_18755</td>
<td align="left">Phosphate ABC transporter (P (ABC)T) permease PstA</td>
<td rowspan="3" align="left">Phosphate transport</td>
</tr>
<tr>
<td align="left">
<italic>pst</italic>B</td>
<td align="center">N4Q52_18760</td>
<td align="left">P (ABC)T ATP-binding protein <italic>Pst</italic>B</td>
</tr>
<tr>
<td align="left">
<italic>pst</italic>S</td>
<td align="center">N4Q52_18745</td>
<td align="left">P (ABC)T substrate-binding protein <italic>Pst</italic>S</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="T5" position="float">
<label>TABLE 5</label>
<caption>
<p>Notable genes identified in iron transport and hormonal modulation.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Genes</th>
<th align="center">Locus Tag</th>
<th align="center">Product</th>
<th align="center">Pathways</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td colspan="4" align="left">Iron transport</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>FbpC</italic>
</td>
<td align="center">N4Q52_20740</td>
<td align="left">Iron (III) transport system ATP-binding protein</td>
<td align="left">Iron (III) transport</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>FeoA</italic>
</td>
<td align="center">N4Q52_20745</td>
<td align="left">ferrous iron transport protein A</td>
<td align="left">Iron (II) transport</td>
</tr>
<tr>
<td colspan="4" align="left">Hormonal modulation</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>TrpA</italic>
</td>
<td align="center">N4Q52_04370</td>
<td align="left">tryptophan synthase subunit alpha</td>
<td rowspan="2" align="left">L-tryptophan production</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>TrpB</italic>
</td>
<td align="center">N4Q52_04365</td>
<td align="left">tryptophan synthase subunit beta</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>MiaA</italic>
</td>
<td align="center">N4Q52_12590</td>
<td align="left">tRNA dimethylallyltransferase</td>
<td rowspan="2" align="left">CK biosynthesis</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>MiaB</italic>
</td>
<td align="center">N4Q52_16645</td>
<td align="left">tRNA-2-methylthio-N6-dimethylallyladenosine synthase</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>SpeA</italic>
</td>
<td align="center">N4Q52_10515</td>
<td align="left">arginine decarboxylase</td>
<td rowspan="2" align="left">Putrescine biosynthesis</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>SpeB</italic>
</td>
<td align="center">N4Q52_10520</td>
<td align="left">Agmatinase</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>SpeD</italic>
</td>
<td align="center">N4Q52_14365</td>
<td align="left">S-adenosylmethionine decarboxylase</td>
<td align="left">Spermidine biosynthesis</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>SpeE</italic>
</td>
<td align="center">N4Q52_14370</td>
<td align="left">Spermidine synthase</td>
<td align="left"/>
</tr>
<tr>
<td align="left">&#x2003;<italic>SpeG</italic>
</td>
<td align="center">N4Q52_02295</td>
<td align="left">Spermidine/Spermine N (1)-acetyltransferase</td>
<td align="left">N1- and N8-acetylspermidine formation</td>
</tr>
<tr>
<td colspan="4" align="left">Nitrogen metabolism</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>NirB</italic>
</td>
<td align="center">N4Q52_04595</td>
<td align="left">nitrite reductase (NADH) large subunit</td>
<td rowspan="2" align="left">Dissimilatory nitrate reduction</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>NirD</italic>
</td>
<td align="center">N4Q52_20880</td>
<td align="left">nitrite reductase (NADH) small subunit</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>AmtB</italic>
</td>
<td align="center">N4Q52_15550</td>
<td align="left">ammonium transporter, Amt family</td>
<td align="left">Ammonia transport</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>UreC</italic>
</td>
<td align="center">N4Q52_09930</td>
<td align="left">urease subunit alpha</td>
<td rowspan="4" align="left">Urea degradation and transport</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>UreG</italic>
</td>
<td align="center">N4Q52_09910</td>
<td align="left">Urease accessory protein UreG</td>
</tr>
<tr>
<td align="left">&#x2003;UreF</td>
<td align="center">N4Q52_09915</td>
<td align="left">Urease accessory protein UreF</td>
</tr>
<tr>
<td align="left">&#x2003;<italic>UreE</italic>
</td>
<td align="center">N4Q52_09925</td>
<td align="left">Urease accessory protein UreE</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap id="T6" position="float">
<label>TABLE 6</label>
<caption>
<p>Notable genes identified for osmotic and oxidative stress.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Genes</th>
<th align="center">Locus Tag</th>
<th align="center">Product</th>
<th align="center">Pathways</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">
<italic>BetB</italic>
</td>
<td align="center">N4Q52_16210</td>
<td align="left">Betaine-aldehyde dehydrogenase</td>
<td align="left">Glycine betaine biosynthesis</td>
</tr>
<tr>
<td align="left">
<italic>ProA</italic>
</td>
<td align="center">N4Q52_16210</td>
<td align="left">Glutamate-5-semialdehyde dehydrogenase</td>
<td align="left"/>
</tr>
<tr>
<td align="left">ProB</td>
<td align="center">N4Q52_15005</td>
<td align="left">Glutamate 5-kinase</td>
<td rowspan="2" align="left">Proline biosynthesis</td>
</tr>
<tr>
<td align="left">ProC</td>
<td align="center">N4Q52_15215</td>
<td align="left">Pyrroline-5-carboxylate reductase</td>
</tr>
<tr>
<td align="left">
<italic>GltB</italic>
</td>
<td align="center">N4Q52_09025</td>
<td align="left">glutamate synthase (NADPH/NADH) large chain</td>
<td rowspan="2" align="left">Glutamate biosynthesis</td>
</tr>
<tr>
<td align="left">
<italic>GltD</italic>
</td>
<td align="center">N4Q52_09020</td>
<td align="left">glutamate synthase (NADPH/NADH) small chain</td>
</tr>
<tr>
<td align="left">
<italic>GlnA</italic>
</td>
<td align="center">N4Q52_21360</td>
<td align="left">Glutamine synthetase</td>
<td align="left"/>
</tr>
<tr>
<td align="left">
<italic>ProX</italic>
</td>
<td align="center">N4Q52_11795</td>
<td align="left">Glycine betaine/proline transport system substrate-binding protein</td>
<td rowspan="3" align="left">Glycine betaine/proline transport system</td>
</tr>
<tr>
<td align="left">
<italic>ProW</italic>
</td>
<td align="center">N4Q52_11800</td>
<td align="left">Glycine betaine/proline transport system permease protein</td>
</tr>
<tr>
<td align="left">
<italic>ProV</italic>
</td>
<td align="center">N4Q52_11805</td>
<td align="left">Glycine betaine/proline transport system ATP-binding protein</td>
</tr>
<tr>
<td align="left">
<italic>GltP</italic>
</td>
<td align="center">N4Q52_22150</td>
<td align="left">proton glutamate symport protein</td>
<td align="left">Glutamate transport</td>
</tr>
<tr>
<td align="left">
<italic>KatE</italic>
</td>
<td align="center">N4Q52_01085</td>
<td align="left">Catalase</td>
<td align="left">Degradation of hydrogen peroxide</td>
</tr>
<tr>
<td align="left">
<italic>Tpx</italic>
</td>
<td align="center">N4Q52_01085</td>
<td align="left">Thiol peroxidase</td>
<td rowspan="2" align="left">Degradation of hydrogen peroxide and organic hydroperoxides</td>
</tr>
<tr>
<td align="left">
<italic>Bcp</italic>
</td>
<td align="center">N4Q52_08155</td>
<td align="left">Peroxiredoxin Q/BCP</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s3-4">
<title>Predicted Secondary Metabolite Cluster Genes Through antiSMASH</title>
<p>The secondary metabolite gene clusters identified for strain AYS9 using antiSMASH analysis are reported in <xref ref-type="table" rid="T7">Table 7</xref>. The identified biosynthetic gene clusters are aerobactin type non-ribosomal peptide siderophore, Stewartan type ladderane, and Colicin type NRPS. The major secondary metabolite gene clusters detected are additional biosynthetic genes, transport-related genes, core biosynthetic genes, regulatory genes, resistance, and other genes (<xref ref-type="fig" rid="F3">Figures 3A, B</xref>). The genes cluster exhibiting 66% and 88% similarity for gene type siderophore and arylpolyene with the most similar known cluster Aerobactin and arylpolygenes node regions 1.1 and 7.1 were also presented (<xref ref-type="table" rid="T7">Table 7</xref>).</p>
<table-wrap id="T7" position="float">
<label>TABLE 7</label>
<caption>
<p>Secondary metabolite gene clusters in the genomes of <italic>Enterobacter mori</italic> strain AYS9.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Node region</th>
<th align="center">Type</th>
<th align="center">From</th>
<th align="center">To</th>
<th align="center">Most similar known cluster</th>
<th align="left"/>
<th align="center">Similarity</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Rg 1.1</td>
<td align="left">Siderophore</td>
<td align="center">1,270,777</td>
<td align="center">1,285,205</td>
<td align="center">Aerobactin</td>
<td align="left">Other</td>
<td align="center">66%</td>
</tr>
<tr>
<td align="left">Rg 4.1</td>
<td align="left">Ladderane</td>
<td align="center">2009</td>
<td align="center">44,567</td>
<td align="center">Stewartan</td>
<td align="left">Saccharide</td>
<td align="center">14%</td>
</tr>
<tr>
<td align="left">Rg 4.2</td>
<td align="left">NRPS</td>
<td align="center">322,675</td>
<td align="center">366,532</td>
<td align="center">Colicin</td>
<td align="left">RiPP</td>
<td align="center">3%</td>
</tr>
<tr>
<td align="left">Rg 5.1</td>
<td align="left">Thiopeptide</td>
<td align="center">130,773</td>
<td align="center">157,075</td>
<td align="center">O-antigen</td>
<td align="left">Saccharide</td>
<td align="center">14%</td>
</tr>
<tr>
<td align="left">Rg 7.1</td>
<td align="left">Arylpolyene</td>
<td align="center">73,134</td>
<td align="center">116,769</td>
<td align="center">Aryl polygenes</td>
<td align="left">Other</td>
<td align="center">88%</td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>
<italic>Enterobacter mori</italic> strain AYS9 biosynthetic gene clusters for secondary metabolites from antiSmash. <bold>(A)</bold> siderophore gene clusters and <bold>(B)</bold> Arylpolene gene clusters.</p>
</caption>
<graphic xlink:href="sjss-13-11302-g003.tif"/>
</fig>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>The goal of the study&#x2019;s design was to identify and describe rhizosphere bacterial strains from the sorghum plant that are capable of stimulating plant development and reducing the effects of drought. A range of hosts, including plants, water, animals, and humans, have been observed to demonstrate an intimate interrelationship with <italic>Enterobacter mori</italic>, which has been isolated from many ecosystems. In general, it has been found that <italic>E. mori</italic>, one of the most prevalent species connected to plants, possesses a number of traits that support plant growth (<xref ref-type="bibr" rid="B30">Jha et al., 2011</xref>). As a result, knowledge based on their environmental and agricultural value in many crops and plants, such as white mulberry (<xref ref-type="bibr" rid="B85">Zhu et al., 2011</xref>), maize (<xref ref-type="bibr" rid="B33">Khan et al., 2022</xref>), and peanut (<xref ref-type="bibr" rid="B39">Ludue&#xf1;a et al., 2019</xref>) has been reported. This is true to a larger extent due to their potential for plant growth promotion. Whole-genome analysis for identifying several <italic>E. mori</italic> genes implicated in PGP characteristics, phytohormones, and stress reduction have not yet been investigated. As a result, we presented the first report on the genomic data for <italic>E. mori</italic>, which was isolated from the sorghum rhizosphere in South Africa.</p>
<p>
<italic>Enterobacter mori</italic> AYS9 was isolated on Luria-Bertani (LB) medium, evaluated on growth-promoting media, and finally sequenced. From both functional and taxonomic data, it was found that the number of genes found in strain AYS9 agrees with those tested in <italic>in vitro</italic> experiments. In addition to the genes that had been previously assessed, other significant genes of agricultural significance were also found. The strain AYS9 might control plant development in a variety of ways, according to the findings of studies that promoted plant growth. For example, in the solubilization of phosphate, IAA and biosynthesis of siderophore. Our results are consistent with past reports on the properties of <italic>Enterobacter</italic> strains and other rhizosphere bacteria associated with the root that promote plant development (<xref ref-type="bibr" rid="B32">K&#xe4;mpfer et al., 2005</xref>; <xref ref-type="bibr" rid="B47">Mukherjee and Roy, 2016</xref>). Strain AYS9 showed the prospects of being able to mitigate drought stress through its ability to withstand exposure to the PEG 6000. Although its growth was observed to be decreasing initially at 5%&#x2013;10% concentration of PEG, it started thriving at 20%&#x2013;30% concentration of PEG. This may be a result of the ability of the rhizobacterium to produce IAA and ACC which has been widely reported to be an important drought-tolerant attribute of rhizobacteria (<xref ref-type="bibr" rid="B22">Fadiji et al., 2022c</xref>).</p>
<p>Microbes&#x2019; capacity to fix atmospheric nitrogen for the use of the plant is dependent on certain enzymes and genes that they generate (<xref ref-type="bibr" rid="B82">Wang et al., 2004</xref>; <xref ref-type="bibr" rid="B59">Peng et al., 2009</xref>). Strain AYS9 was found to contain the nitrite reductase enzyme, which codes for by the genes <italic>nirB</italic> and <italic>nirD</italic> involved in the dissimilatory nitrate reduction pathway. Other genes discovered are involved in the transport of ammonia (<italic>amtB</italic>) and urea (<italic>ureC</italic>, <italic>ureG</italic>, <italic>ureF</italic>, and <italic>ureE</italic>), which may increase the amount of nitrogen in the soil. This outcome is comparable to one from a previous investigation in which flavodoxin and the ammonia transport gene (<italic>amtB</italic>) were found in MSR2 genome (<xref ref-type="bibr" rid="B48">Nascimento et al., 2020a</xref>).</p>
<p>The potential of strain AYS9 to dissolve phosphate under <italic>in vitro</italic> conditions on tricalcium media was verified by the discovery of many phosphate solubilization and transport-related genes. In a variety of bacterial phyla, gluconic acid (GA) is recognized as a precursor that promotes the solubilization of phosphate. Microbial activities and uses have been influenced by the production of GA by the enzyme glucose-1-dehydrogenase and its nonprotein chemical component pyrroloquinolone quinine (pqq) (<xref ref-type="bibr" rid="B60">Ramachandran et al., 2006</xref>). Despite the absence of <italic>pqq</italic> genes in AYS9 strain, investigations have revealed that the diazotroph bacterial endophyte <italic>Herbaspirillum seropedicae</italic> Z67 connected to commercial plants expresses heterologous <italic>pqq</italic> genes (<italic>pqqABCDEF</italic>) that exhibit phosphate solubilization capacity (<xref ref-type="bibr" rid="B81">Wagh et al., 2014</xref>). Similar to this, <italic>Klebsiella</italic> sp. D5A&#x2019;s genome was also found to be devoid of <italic>pqq</italic> genes (<xref ref-type="bibr" rid="B24">Guerrieri et al., 2021</xref>). Due to their high affinity and the presence of phosphate transport genes <italic>pstABCS</italic>, found in strain AYS9 may be better able to absorb phosphates. These results support those made earlier by <xref ref-type="bibr" rid="B24">Guerrieri et al. (2021)</xref> and <xref ref-type="bibr" rid="B72">Shariati J et al. (2017)</xref> regarding the phosphate transport genes <italic>pstABCS</italic> expression, on the WG analysis of <italic>Klebsiella variicola</italic> UC4115 and <italic>Pantoea agglomerans</italic> P5 respectively. Phosphorus absorption by soil and plant bioavailability may both be improved by the presence of <italic>pst</italic> genes. The discovery of the <italic>phoA</italic> gene, which codes for the alkaline phosphatase enzyme involved in numerous phosphorus metabolic processes including phosphate assimilation, was also present in strain AYS9, which was also consistent with the findings for <italic>Burkholderia multivorans</italic> WS-FJ9 genome (<xref ref-type="bibr" rid="B37">Liu et al., 2020</xref>). In addition, the discovery of the genes <italic>ppx, pgl</italic> and <italic>pgl</italic> in the AYS9 genome, which respectively encodes for 6-phosphogluconolactonase and exoployphosphatase for the synthesis of d-gluconate and inorganic pyrophosphatase degradation, may have influenced the bacterial strain&#x2019;s capacity to solubilize phosphate in the plant&#x2019;s rhizosphere. Our findings, however, are consistent with those made by (<xref ref-type="bibr" rid="B49">Nascimento et al., 2020b</xref>), who found that the genome of <italic>Bacillus megaterium</italic> STB1 contains <italic>phoAD</italic> genes that boost the bacterial strain&#x2019;s capacity to solubilize phosphate.</p>
<p>The expression of genes active in the synthesis of IAA and siderophore was found in the rhizosphere bacterial strain AYS9, which is consistent with earlier studies on the PGP traits of rhizobacteria (<xref ref-type="bibr" rid="B59">Peng et al., 2009</xref>; <xref ref-type="bibr" rid="B76">Tariq et al., 2014</xref>). It has been hypothesized that many pathways, including tryptamine, indole-3-acetonitrile (IAN), indole-3-acetamide, and indole-3-pyruvate (IPA), are involved in the production of IAA in plants and microbes (<xref ref-type="bibr" rid="B73">Spaepen and Vanderleyden, 2011</xref>). IAA, a key auxin found in plants, may influence gene expression and biosynthesis in microbes via signaling. Therefore, the production of auxin signal molecules by the microbes may be related to plant responses against naturally occurring harmful pathogens (<xref ref-type="bibr" rid="B73">Spaepen and Vanderleyden, 2011</xref>; <xref ref-type="bibr" rid="B22">Fadiji et al., 2022c</xref>). In addition, the identical functions of the <italic>ipdC</italic> gene in <italic>Enterobacter cloacae</italic> have been discovered (<xref ref-type="bibr" rid="B34">Koga et al., 1991</xref>) but were not observed in the genome of AYS9.</p>
<p>It&#x2019;s interesting to note that strain AYS9 has tryptophan synthase, which is irreversibly implicated in the pyridoxal phosphate pathway and reversibly catalyzes the condensation of serine and indole to create glyceraldehyde-3-phosphate from indole-3-glycerol phosphate (<xref ref-type="bibr" rid="B28">Ireland et al., 2008</xref>). The production of IAA by bacteria through the IAN route may be aided by the presence of amidase enzymes. Furthermore, strain AYS9&#x2019;s participation in two distinct IAA metabolic pathways demonstrated their capacity to produce IAA, which is essential for the creation and growth of plant roots. The AYS9 genome was then found to harbour <italic>miaAB</italic> genes involved in cytokinin production and transformation. The bacterial genome contains enzyme genes for tRNA dimethylallyltransferases that may improve the generation of iPR&#x2014;N6-(dimethylallyl) adenosine.</p>
<p>In the <italic>Pantoea phytobeneficialis</italic> MSR2 genome, various cytokinin genes, such as <italic>miaA</italic> and <italic>miaB</italic>, are expressed. These genes change <italic>Ipr</italic> to 2-methylthio-N6-(dimethylallyl) adenosine and then to 2-methylthio-cis-ribozeatin (<xref ref-type="bibr" rid="B48">Nascimento et al., 2020a</xref>). The immediate effects of this specific gene on plant growth promotion imply that cytokinin production may be crucial for promoting plant health and growth (<xref ref-type="bibr" rid="B83">Wani et al., 2016</xref>). Despite this, reports on cytokinin genes from this rhizobacterium strain AYS9 are not yet published, necessitating future comparative studies into agriculturally significant <italic>E. mori</italic> strain AYS9 to learn more about their unique genes. Plant development may be aided by the identification of siderophore and iron-related genes in the <italic>E. mori</italic> strain AYS9. These genes may increase the accessibility of plants to the soil&#x2019;s mineral resources. A crucial function in the mineralization of insoluble iron and its bioavailability for plant use may be played by iron transport genes identified in strain AYS9. Additionally, the bacteria&#x2019;s ability to produce 2,3-butanediol, induce systemic resistance and increase tolerance of the plant to drought have all been connected to their capacity for biocontrol (<xref ref-type="bibr" rid="B41">Madhaiyan et al., 2010</xref>; <xref ref-type="bibr" rid="B63">Samaras et al., 2021</xref>).</p>
<p>The pathogen-suppressing abilities of rhizobacteria depend on their capacity to create biocontrol agents. Rhizobacteria have used indirect processes in the creation of metabolic chemicals to control phytopathogens (<xref ref-type="bibr" rid="B65">Santoyo et al., 2016</xref>; <xref ref-type="bibr" rid="B56">Orozco-Mosqueda et al., 2021</xref>). It is possible that siderophore production, which increases the strain AYS9&#x2019;s antibiosis activity against plant pathogens, is the cause of the strain&#x2019;s capacity for biocontrol and stress reduction (<xref ref-type="bibr" rid="B42">Maheshwari et al., 2019</xref>). It has been determined that the siderophore catecholate present in the bacterial genome is crucial for bacterial adhesion to receptor surfaces, transport and iron chelation (<xref ref-type="bibr" rid="B58">Pedraza et al., 2010</xref>). In strain AYS9, iron transport-related genes like <italic>fbpC</italic> and <italic>feoA</italic> were discovered. Contrary to earlier findings, no prominent genes involved in siderophore formation and transport that are necessary for the change of chorismate into enterobactin, such as <italic>fepABCDG</italic> and <italic>entABCDEFGHS</italic> (<xref ref-type="bibr" rid="B25">Hubrich et al., 2021</xref>), we observed in this present study.</p>
<p>The quantity of intracellular polyamines is controlled by production, breakdown, excretion, and absorption from the environment (<xref ref-type="bibr" rid="B35">Kurihara et al., 2011</xref>). L-arginine is converted into putrescine via processes that are catalyzed by the enzyme&#x2019;s arginine decarboxylase and agmatinase. The <italic>speA</italic> and <italic>speB</italic> genes encode these enzymes. The two ornithine-decarboxylation enzymes (OCDs), which are either encoded by <italic>speC</italic> or <italic>speF</italic>, may also convert L-ornithine into putrescine (<xref ref-type="bibr" rid="B35">Kurihara et al., 2011</xref>; <xref ref-type="bibr" rid="B68">Schneider and Wendisch, 2011</xref>). Putrescine and decarboxylated S-adenosylmethionine (SAM) served as the building blocks for the production of spermidine, which needs the enzymes <italic>speD</italic> and <italic>speE</italic> and were identified in this AYS9 strain. Although it is unclear how these biosynthetic activities are controlled, the intracellular concentration of spermidine appears to be self-regulated (<xref ref-type="bibr" rid="B70">Shah and Swiatlo, 2008</xref>).</p>
<p>Plant sensitivity to heat or cold shock may be improved by the presence of osmotic stress-regulating genes. Similarly, to this, the protein-coding genes that control the effects of heat and cold stimuli can work through several gene families and differentiating regulations (<xref ref-type="bibr" rid="B83">Wani et al., 2016</xref>). The strain AYS9 included genes such as <italic>betB</italic>, a component of the glycine betaine biosynthesis pathway known for its osmoprotective properties. This supports past research on <italic>Bacillus substilis</italic> (<xref ref-type="bibr" rid="B10">Boch et al., 1996</xref>; <xref ref-type="bibr" rid="B27">Hussain Wani et al., 2013</xref>). Also, genes such as <italic>proB</italic> and <italic>proC</italic> involved in proline biosynthesis were identified in the strain AYS9. Additionally, strain AYS9 included genes related to proline biosynthesis, including <italic>proB</italic> and <italic>proC,</italic> which is one of the notable mechanisms used by beneficial microbes for the mitigation of drought stress. Pyroline-5-carboxylate synthetase (<italic>P5CS1</italic>), a stress-induced gene in <italic>Arabidopsis</italic>, limits L-proline incorporation in chloroplasts (<xref ref-type="bibr" rid="B75">Strizhov et al., 1997</xref>; <xref ref-type="bibr" rid="B74">Stein et al., 2011</xref>; <xref ref-type="bibr" rid="B19">Fadiji et al., 2021</xref>).</p>
<p>In any living creature, glutamine and glutamate act as the primary amino group donors for all nitrogen-containing substances, such as other amino acids and the building blocks for the creation of RNA and DNA. The strain AYS9 has genes for the production and transport of glutamate, including <italic>gltB</italic>, <italic>gltD</italic>, and <italic>gltP</italic>. Glutamate serves as a key intracellular potassium antagonist in addition to its involvement in anabolism (<xref ref-type="bibr" rid="B45">McLaggan et al., 1994</xref>). Additionally, certain bacteria and archaea use it as an osmoprotectant (<xref ref-type="bibr" rid="B67">Saum et al., 2006</xref>). Our findings are consistent with a previous study on <italic>B. subtilis</italic>, in which it was shown that glutamate is the precursor to proline, which is present in molar quantities in hyperosmotic circumstances and acts as a compatible solute to protect the cells (<xref ref-type="bibr" rid="B12">Brill et al., 2011</xref>).</p>
<p>In this strain AYS9 genome, it was discovered that <italic>KatE</italic>, which encodes catalase and is involved in the breakdown of hydrogen peroxide, was present. The transgenic indica rice cultivar is more tolerant to salt stress when the catalase genes are overexpressed in <italic>E. coli</italic> (<xref ref-type="bibr" rid="B46">Moriwaki et al., 2008</xref>). Additionally, <italic>Escherichia coli</italic> strain K12 catalase gene expression increases the jute plant&#x2019;s resistance to salt stress (<xref ref-type="bibr" rid="B29">Islam et al., 2013</xref>). Furthermore, the genome of strain AYS9 had the thiol peroxidase gene, which was shown to degrade organic hydroperoxides and hydrogen peroxide. This gene is well-known for its function in the biocontrol of wheat blast by <italic>Bacillus</italic> spp. This function is related to induced systemic resistance and the generation of antimicrobial chemicals in host plants like tomatoes (<xref ref-type="bibr" rid="B6">Baier and Dietz, 1996</xref>; <xref ref-type="bibr" rid="B18">El-Gaied et al., 2013</xref>).</p>
</sec>
<sec sec-type="conclusion" id="s5">
<title>Conclusion</title>
<p>In-depth Information on the prominent plant growth-promoting genes present in <italic>E. mori</italic> AYS9 with diverse roles and potential to mitigate drought were explored in this study. Some significant regulatory and plant growth-promoting genes were discovered by genome analysis. Notable genes that encourage plant development were found in <italic>E. mori</italic>. Their importance and promise in agriculture cannot be underestimated. The numerous genes discovered had biotechnological significance in the interactions between microorganisms and plants, in plant resistance to environmental stress (drought, osmotic and oxidative), and in organic compounds that could improve soil health and plant growth and the yield of the crop. The existence of these notable genes has important implications for understanding <italic>E. mori</italic> AYS9&#x2019;s genome PGP activities alongside showing promise in establishing sustainable agriculture. Additionally, according to the data on <italic>E. mori</italic> AYS9, future research is encouraged to take advantage of its potential as a prospective option for creating bioinoculants to deal with abiotic stress-related agricultural issues in the future, most importantly through field trials.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s6">
<title>Data Availability Statement</title>
<p>The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/supplementary material.</p>
</sec>
<sec id="s7">
<title>Author Contributions</title>
<p>AF, AA, and OB conceived the ideas. AF collected the data and developed the manuscript. AA and OB provided technical input and proofread the manuscript. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec id="s8">
<title>Funding</title>
<p>The study was funded by the National Research Foundation, South Africa (UID123634 and UID132595) awarded to OB.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<ack>
<p>AF and AA gratefully acknowledged the North-West University for a Postdoctoral fellowship. OB appreciates the research grant (UID132595) that has supported this research.</p>
</ack>
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