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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">4</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:27D7DBB2-BDE1-5A1F-B26F-1372106F69DB</journal-id>
      <journal-id journal-id-type="aggregator">urn:lsid:zoobank.org:pub:D281A135-8CF2-44EB-843A-86285A8FE340</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">BioRisk</journal-title>
        <abbrev-journal-title xml:lang="en">BR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">1313-2644</issn>
      <issn pub-type="epub">1313-2652</issn>
      <publisher>
        <publisher-name>Pensoft Publishers</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3897/biorisk.20.97581</article-id>
      <article-id pub-id-type="publisher-id">97581</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="biological_taxon">
          <subject>Bacteria</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Ecology &amp; Environmental sciences</subject>
        </subj-group>
        <subj-group subj-group-type="geographical_area">
          <subject>Europe</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>﻿Study of the plant growth-promoting capacity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 in a model plant system</article-title>
      </title-group>
      <contrib-group content-type="authors">
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Georgieva</surname>
            <given-names>Gloria</given-names>
          </name>
          <email xlink:type="simple">gloriq_georgieva1@abv.bg</email>
          <xref ref-type="aff" rid="A1">1</xref>
          <xref ref-type="aff" rid="A2">2</xref>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
          <role content-type="http://credit.niso.org/contributor-roles/methodology/">Methodology</role>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Nedeva</surname>
            <given-names>Trayana</given-names>
          </name>
          <uri content-type="orcid">https://orcid.org/0000-0002-5164-6659</uri>
          <xref ref-type="aff" rid="A1">1</xref>
          <role content-type="http://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
          <role content-type="http://credit.niso.org/contributor-roles/writing-original-draft/">Writing - original draft</role>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Badalova</surname>
            <given-names>Marina</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Deleva</surname>
            <given-names>Veronika</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Savov</surname>
            <given-names>Valentin</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
          <role content-type="http://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">Department of General and Industrial Microbiology, Faculty of Biology, Sofia University St. Kliment Ohridski, 8 Dragan Tzankov Str., Sofia 1164, Bulgaria</addr-line>
        <institution>ROMB LTD</institution>
        <addr-line content-type="city">Sofia</addr-line>
        <country>Bulgaria</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">ROMB LTD, 1 “Aboba” St. 1606, Sofia, Bulgaria</addr-line>
        <institution>Sofia University "St. Kliment Ohridski"</institution>
        <addr-line content-type="city">Sofia</addr-line>
        <country>Bulgaria</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Gloria Georgieva (gloria.georgievaa@gmail.com)</p>
        </fn>
        <fn fn-type="edited-by">
          <p>Academic editor: V. Petrova</p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2023</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>15</day>
        <month>05</month>
        <year>2023</year>
      </pub-date>
      <volume>20</volume>
      <fpage>115</fpage>
      <lpage>128</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/E1D15471-9C4E-5562-9823-DA3E762542D1">E1D15471-9C4E-5562-9823-DA3E762542D1</uri>
      <history>
        <date date-type="received">
          <day>15</day>
          <month>11</month>
          <year>2022</year>
        </date>
        <date date-type="accepted">
          <day>06</day>
          <month>02</month>
          <year>2023</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Gloria Georgieva, Trayana Nedeva, Marina Badalova, Veronika Deleva, Valentin Savov</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <abstract>
        <label>﻿Abstract</label>
        <p>Plant Growth Promoting Rhizobacteria (<abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0EQE">PGPR</abbrev>) represent a microbial community that exerts growth-promoting capabilities in plants by various mechanisms. Among the <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0EUE">PGPR</abbrev> genera, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part></tp:taxon-name></italic> spp. deserves special attention. It is due to its characteristic traits, like the production of phytohormones and siderophores, solubilization of minerals and phosphates, and plant protection from biotic and abiotic stress. These <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0E6E">PGPR</abbrev> properties depend on the microorganism and its plant counterpart. The use of microbial strains as bioinoculants must consider the physiological and economic aspects of the process, and the plant growth stimulating effect has to be checked and proved. This study aimed to explore the <abbrev xlink:title="plant growth-promoting" id="ABBRID0EDF">PGP</abbrev> capacity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain in a model plant system of the economically important corn culture (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name></italic>). The effect of the strain’s metabolic status on the plant germination capacity was evaluated. Bacterial cultures, grown 16 h and 48 h, were explored for the treatment of the corn seeds at three experimental concentrations: 0.1, 0.2, and 0.4%, and monitoring of their germination capacity through the growth indicators length of the radicle, length of the coleoptile, and the number of lateral roots. The data obtained outline the positive effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 on the germination capacity of corn when applied at 0.2% concentration. The <italic>in vitro</italic> treatment of the model plants with 0.2% suspension resulted in a 22.87%–28.33% increase in the length of the radicle, a 35.96%–49.56% increase in the length of the coleoptile, and a 5.41–16.67% increase in the number of the lateral roots. High values of the vigour index (2125 for 16 h and 2721 for 48 h culture) were also registered. The strain’s ability to produce siderophores of hydroximate type and exhibit phosphate solubilizing activity is proved. The optimal treatment parameters of the corn seeds comprise the application of 0.2% suspension of 16 h grown <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain for five days.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>biofertilizer</kwd>
        <kwd>PGPR</kwd>
        <kwd>rhizosphere microorganisms</kwd>
        <kwd>
          <italic>
            <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name>
          </italic>
        </kwd>
      </kwd-group>
    </article-meta>
    <notes>
      <sec sec-type="Citation" id="SECID0ELH">
        <title>Citation</title>
        <p>Georgieva G, Nedeva T, Badalova M, Deleva V, Savov V (2023) Study of the plant growth-promoting capacity of <italic>Pseudomonas putida</italic> 1046 in a model plant system. In: Chankova S, Danova K, Beltcheva M, Radeva G, Petrova V, Vassilev K (Eds) Actual problems of Ecology. BioRisk 20: 115–128. <ext-link xlink:type="simple" ext-link-type="doi" xlink:href="10.3897/biorisk.20.97581">https://doi.org/10.3897/biorisk.20.97581</ext-link></p>
      </sec>
    </notes>
  </front>
  <body>
    <sec sec-type="﻿Introduction" id="SECID0ECAAC">
      <title>﻿Introduction</title>
      <p>The soil microbial communities influence plant growth and development. The playground for this effect is the rhizosphere since the plant root system and the soil microorganisms interact there. This interaction is a complex process influenced by various environmental factors, such as temperature, humidity, pH, availability of nutrients, etc. (<xref ref-type="bibr" rid="B16">Mimmo et al. 2018</xref>). The plant-associated bacteria can execute beneficial or deleterious effects on plant growth (<xref ref-type="bibr" rid="B5">Dobbelaere et al. 2003</xref>). The soil bacteria that positively affect the plant are called Plant Growth Promoting Rhizobacteria (<abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0EQAAC">PGPR</abbrev>) (<xref ref-type="bibr" rid="B13">Kloepper and Schroth 1978</xref>). <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0EYAAC">PGPR</abbrev> constitute a vital component of the rhizosphere. They support the development of the plant’s root and shoot systems. <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0E3AAC">PGPR</abbrev> positively affect plant morphogenesis, flowering, and photosynthesis efficiency (<xref ref-type="bibr" rid="B11">Hossain et al. 2017</xref>).</p>
      <p>The need for environmentally friendly fertilizers or biofertilizers is constantly increasing nowadays (<xref ref-type="bibr" rid="B15">Meliani et al. 2017</xref>) on account of soil, water, and air contamination due to chemicals such as fertilizers and pesticides. A few alternatives to fertilizers that are environmentally friendly have been developed (<xref ref-type="bibr" rid="B10">Gupta et al. 2015</xref>). Thus, the impact of <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0EOBAC">PGPR</abbrev> on agriculture steadily increases as they offer an attractive way to replace chemical products. Fertilizers containing microorganisms are an appropriate alternative to chemical ones since they are a natural component of healthy soil that enriches rather than pollutes it (<xref ref-type="bibr" rid="B22">Vessey 2003</xref>; <xref ref-type="bibr" rid="B19">Nadeem et al. 2016</xref>). Moreover, they produce growth-promoting substances in large quantities that influence the plant’s morphology (<xref ref-type="bibr" rid="B3">Bhattacharyya and Jha 2012</xref>).</p>
      <p>Many species belonging to g. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part></tp:taxon-name></italic> possess plant growth-promoting (<abbrev xlink:title="plant growth-promoting" id="ABBRID0EHCAC">PGP</abbrev>) characteristics that allow their application as bacterial fertilizers. They are abundantly present in the rhizosphere. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part></tp:taxon-name></italic> spp. are known for their well-established growth-promoting mechanisms. They encompass better root colonization, the production of enzymes, metabolites, phytohormones and siderophores, mineral and phosphate solubilization, and plant protection from biotic and abiotic stress (<xref ref-type="bibr" rid="B19">Nadeem et al. 2016</xref>).</p>
      <p>The application of the microbial <abbrev xlink:title="plant growth-promoting" id="ABBRID0EYCAC">PGP</abbrev> properties depends on the microorganism and its plant counterpart. Corn (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name></italic>) is one of the most important cereal crops in the world after wheat and rice. It is used as livestock feed, human food, and raw material for several industries (<xref ref-type="bibr" rid="B14">Kumar and Jhariya 2013</xref>). The corn growth, development, and yield are well-focused biotechnological targets, and the plant attributes, such as germination rate, drought tolerance, and yield components, are objects of profound research and technological interest. <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0ELDAC">PGPR</abbrev> could be used for maximizing these parameters and applied as a potent tool in sustainable agriculture. The contribution of g. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part></tp:taxon-name></italic> representatives in the enhancement of some biochemical and agronomic parameters of corn under normal conditions or exposure to various abiotic stress is well-recognized in the literature (<xref ref-type="bibr" rid="B18">Mubeen et al. 2021</xref>). However, the use of pseudomonads and their corn counterpart in biofertilization programs must consider the physiological and economic aspects of the process, and the plant growth stimulating effect has to be checked and proved.</p>
      <p>This study aimed to explore the <abbrev xlink:title="plant growth-promoting" id="ABBRID0E3DAC">PGP</abbrev> capacity of bacteria belonging to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> species in a model plant system of the economically important corn culture <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name></italic>.</p>
    </sec>
    <sec sec-type="materials|methods" id="SECID0EWEAC">
      <title>﻿Materials and methods</title>
      <sec sec-type="﻿Bacterial strain and test plants" id="SECID0E1EAC">
        <title>﻿Bacterial strain and test plants</title>
        <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain was used in this study. It possesses the biochemical capacity to catabolize aromatic hydrocarbons and their derivatives. Corn seeds (Dekalb – DKC 5830 HD (Hybrid 101)) were used as a model plant test system. They are characterized by a fast initial development, high quality of the grain, tolerance to high sowing norms, and a response to high fertilizers and sowing norms. In some of the experiments, soybean seeds (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Glycine">Glycine</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="max">max</tp:taxon-name-part></tp:taxon-name></italic> L.) were used.</p>
      </sec>
      <sec sec-type="﻿Culture media and cultivation conditions" id="SECID0EWFAC">
        <title>﻿Culture media and cultivation conditions</title>
        <p>The experimental strain was maintained on Nutrient agar (BB-NCIPD Ltd., Bulgaria). Batch cultures in Nutrient broth were obtained after cultivation at 28 °C for 16 h or 48 h on a rotary shaker (220 rpm).</p>
      </sec>
      <sec sec-type="﻿Biochemical analysis" id="SECID0E2FAC">
        <title>﻿Biochemical analysis</title>
        <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 biochemical profile was established applying ApiZYM rapid systems for the detection of bacterial enzymes and Api 20 NE standardized system for the identification of non-fastidious, non-enteric Gram-negative rods. The tests performance was according to the methods described by <xref ref-type="bibr" rid="B12">Humble et al. (1977)</xref> and <xref ref-type="bibr" rid="B6">Donnelly (2006)</xref>. Siderophore detection was performed following the method of <xref ref-type="bibr" rid="B1">Alexander and Zuberer (1991)</xref>. The assay for phosphate solubilization was done according to Shahid et at. (2015).</p>
      </sec>
      <sec sec-type="﻿PGP effect determination" id="SECID0EYGAC">
        <title>PGP effect determination</title>
        <p>The seed germination method was applied to study the <abbrev xlink:title="plant growth-promoting" id="ABBRID0E5GAC">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain on corn (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name></italic>) seeds. The corn seeds were subjected to surface sterilization before the germination test. Sodium hypochlorite (0.02%) solution was applied for 2 min., followed by intense rinsing with sterile distilled water. The seeds’ germination capacity was assessed through the growth parameters of the plant root system (<xref ref-type="bibr" rid="B20">Sharma et al. 2014</xref>). Water suspensions with a defined concentration of 0.1%, 0.2%, and 0.4% were prepared from the 16 h and 48 h test microorganisms containing 10<sup>8</sup> CFU/ml. The corn seeds were immersed in these suspensions and cultured for five days at 25 °C. The growth parameters: length of the radicle, length of the coleoptile, and the number of lateral roots were measured. The positive effect of the test strain on the germination capacity of the corn plants was calculated as a percentage of untreated control. The plant vigour index was also calculated using the following formula: Vigour index = (mean radicle length + mean coleoptile length) × % germination (<xref ref-type="bibr" rid="B2">Baki et al. 1973</xref>). To prove the relationship (and its strength) between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046, and the growth parameters of the plant root system the seed germination method was applied to another technical crop, soybean (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Glycine">Glycine</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="max">max</tp:taxon-name-part></tp:taxon-name></italic> L.), at the same experimental conditions. Each treatment was performed following a completely randomized design with three replicates and 10 seeds/replicate.</p>
      </sec>
      <sec sec-type="﻿Correlation analysis" id="SECID0EYIAC">
        <title>﻿Correlation analysis</title>
        <p>Correlation analysis was performed by calculating the correlation coefficients with MS Excel software of two variables data sets – <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 suspension concentration (0% (control), 0.1%, and 0.2%) and the growth parameters of the plant root system (the indices length of the radicle, length of the coleoptile, the number of the lateral roots, and the vigour index).</p>
      </sec>
      <sec sec-type="﻿Data analyses" id="SECID0EJJAC">
        <title>﻿Data analyses</title>
        <p>All presented data are mean values of at least 3 individual experiments. The data were analysed by MS EXCEL build-in function, and the results were presented as means with standard deviations (n=3).</p>
      </sec>
    </sec>
    <sec sec-type="﻿Results" id="SECID0EOJAC">
      <title>﻿Results</title>
      <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain has been selected on the basis of preliminary biochemical analyses that indicate its potential plant growth-promoting capacity. The biochemical profile of the strain was established applying ApiZYM and Api 20 NE detection systems. The biochemical profile data presented in Table <xref ref-type="table" rid="T1">1</xref> showed activity of the enzymes alkaline phosphatase, acid phosphatase, and naphthol-AS-BI-phosphohydrolase, indicative for <abbrev xlink:title="plant growth-promoting" id="ABBRID0EDKAC">PGP</abbrev> potential due to their involvement in the phosphate solubilization and mineralization. Additional phytohormones analysis showed the biosynthetic capacity of the test strain for the phytohormones gibberellic acid (<abbrev xlink:title="phytohormones gibberellic acid" id="ABBRID0EHKAC">GA3</abbrev>), indole acetic acid (<abbrev xlink:title="indole acetic acid" id="ABBRID0ELKAC">IAA</abbrev>), and jasmonic acid (data not shown).</p>
      <table-wrap id="T1" position="float" orientation="portrait">
        <label>Table 1.</label>
        <caption>
          <p>Biochemical characterization of the <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain.</p>
        </caption>
        <table id="TID0EZVAE" rules="all">
          <tbody>
            <tr>
              <th rowspan="1" colspan="2">ApiZYM</th>
              <th rowspan="1" colspan="2">Api 20NE</th>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Alkaline phosphatase</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">NO<sub>3</sub> Reduction of nitrates to nitrites</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Esterase (C 4)</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">Reduction of nitrates to nitrogen</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Esterase Lipase (C 8)</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">TRP Indole production (tryptophan)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Lipase (C 14)</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">GLU Fermentation (glucose)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Leucine arylamidase</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">ADH Arginine dihydrolase</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Valine arylamidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">URE Urease</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Cystine arylamidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">ESC Hydrolysis (βglucosidase) (esculin)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Trypsin</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">GEL Hydrolysis (protease) (gelatin)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">α-chimotrypsin</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">PNGP β-Galactosidase (paranitropheny l-ßDgalactopyranosidase)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Acid phosphatase</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">GLU Assimilation (glucose)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">Naphthol-AS-BI-phosphohydrolase</td>
              <td rowspan="1" colspan="1">positive</td>
              <td rowspan="1" colspan="1">ARA Assimilation (arabinose)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">α-galactosidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">MNE Assimilation (mannose)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">β- galactosidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">MAN Assimilation (mannitol)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">β-glucuronidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">NAG Assimilation (N-acetylglucosamine)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">α-glucuronidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">MAL Assimilation (maltose)</td>
              <td rowspan="1" colspan="1">negative</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">β-glucosidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">GNT Assimilation (potassium gluconate)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">N-acetyl-β-glucosaminidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">CAP Assimilation (capric acid)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">α-mannosidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">ADI Assimilation (adipic acid)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1">α-fucosidase</td>
              <td rowspan="1" colspan="1">negative</td>
              <td rowspan="1" colspan="1">MLT Assimilation (malate)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1">CIT Assimilation (trisodium citrate)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1">PAC Assimilation (phenylacetic acid)</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
            <tr>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1"/>
              <td rowspan="1" colspan="1">OX Cytochrome oxidase</td>
              <td rowspan="1" colspan="1">positive</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>The effect of the strain metabolic status on the test plants’ germination was evaluated in order to check the <abbrev xlink:title="plant growth-promoting" id="ABBRID0ESEAE">PGP</abbrev> capacity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain. The <abbrev xlink:title="plant growth-promoting" id="ABBRID0EBFAE">PGP</abbrev> capacity of the bacterial strain was assessed in respect to its test plants. The seeds germination of the test plants was used as an assessment indicator through the quantitative measurement of three indices: length of the radicle, length of the coleoptile, and number of lateral roots. The corn seeds at three experimental concentrations (0.1, 0.2, and 0.4%) were treated with bacterial cultures, grown for 16 h and 48 h and monitored for their germination capacity. The length of the radicle, length of the coleoptile, and the number of lateral roots were used as growth indicators.</p>
      <sec sec-type="﻿Length of the radicle" id="SECID0EFFAE">
        <title>﻿Length of the radicle</title>
        <p>The values for the growth indicator length of the radicle are shown in Figs <xref ref-type="fig" rid="F1">1A</xref>, <xref ref-type="fig" rid="F2">2</xref>. They indicate a positive effect of the bacterial culture on the plant physiology, best represented during the treatment with 0.2% suspension. An increase of 22.87% for the 16 h culture and 28.33% for the 48 h one was observed. The values for the remaining two tested concentrations (0.1% and 0.4%) showed variations in the range of 1.7 to 9.9% compared to the untreated control.</p>
        <fig id="F1" position="float" orientation="portrait">
          <object-id content-type="arpha">099BC68B-9366-569A-B1BA-C149135515BB</object-id>
          <label>Figure 1.</label>
          <caption>
            <p><abbrev xlink:title="plant growth-promoting" id="ABBRID0E2FAE">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 on the germination of corn seeds evaluated through length of the radicle (<bold>A</bold>), length of the coleoptile (<bold>B</bold>), and the number of lateral roots (<bold>C</bold>).</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g001.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849442.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849442</uri>
          </graphic>
        </fig>
        <fig id="F2" position="float" orientation="portrait">
          <object-id content-type="arpha">0772C63B-5423-5EE0-B270-0104355730B1</object-id>
          <label>Figure 2.</label>
          <caption>
            <p>Visual representation of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 <abbrev xlink:title="plant growth-promoting" id="ABBRID0EIHAE">PGP</abbrev> effect on corn seeds germination capacity.</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g002.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849443.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849443</uri>
          </graphic>
        </fig>
      </sec>
      <sec sec-type="﻿Length of the coleoptile" id="SECID0ERHAE">
        <title>﻿Length of the coleoptile</title>
        <p>The data for the length of the coleoptile show that all three tested concentrations exhibit a positive effect on its growth (Figs <xref ref-type="fig" rid="F1">1B</xref>, <xref ref-type="fig" rid="F2">2</xref>). The values indicated an increase in this growth parameter between 17.4% and 49.6%. The tendency for the best stimulatory effect of 0.2%, acknowledged for the length of the radicle, was also observed here. An increase of 35.96% for the 0.2% and 49.56% for 0.4% suspensions was registered, respectively. Comparing the physiological status of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">P.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> culture, it is evident that at 0.1%, the stimulatory effect was the same (11.7%) regardless of the culture age. With the increase of the bacterial strain concentration (0.2% and 0.4%), the 48 h population stimulated the coleoptile development more efficiently (10% to 15%) compared to the 16 h one.</p>
      </sec>
      <sec sec-type="﻿Number of the lateral roots" id="SECID0EKIAE">
        <title>﻿Number of the lateral roots</title>
        <p>The third index (number of the lateral roots), used for assessment of the corn germination capacity, showed a relatively lower stimulatory effect (2.78%–18.60%) as compared to the previous two indicators. However, it is evident that the tendency for the highest positive results obtained by the 0.2% suspension of the bacterial strain is kept (Figs <xref ref-type="fig" rid="F1">1C</xref>, <xref ref-type="fig" rid="F2">2</xref>). The 16 h bacterial culture showed higher growth promotion of the lateral roots compared to the 48 h (16.67% vs. 5.41%).</p>
        <p>Among the three tested bacterial concentrations, the 0.2% suspension was the right choice for the seeds’ treatment. The 0.1% expressed no or mild positive effect on the number of lateral roots and the length of radicles, as shown in Figs <xref ref-type="fig" rid="F1">1</xref>, <xref ref-type="fig" rid="F2">2</xref>. Compared to the 0.2%, the highest tested concentration of 0.4% did not significantly affect any of the analysed indices.</p>
      </sec>
      <sec sec-type="﻿Vigour index" id="SECID0ECJAE">
        <title>﻿Vigour index</title>
        <p>The values for the vigour index are presented in Fig. <xref ref-type="fig" rid="F3">3</xref>. The corn plants were treated with 0.1%, 0.2%, and 0.4% suspensions of 16 h and 48 h <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">P.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> culture and evaluated five days after <italic>in vitro</italic> germination. The highest values of the vigour index were registered after treatment with 0.2% suspension of the bacterial strain: 2125 for 16 h and 2721 for 48 h culture.</p>
        <fig id="F3" position="float" orientation="portrait">
          <object-id content-type="arpha">C004F9F5-721E-587B-BF42-0B1548A5B53C</object-id>
          <label>Figure 3.</label>
          <caption>
            <p>Effect of bacterial inoculation on corn vigour index after 5 days <italic>in vitro</italic> germination.</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g003.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849444.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849444</uri>
          </graphic>
        </fig>
      </sec>
      <sec sec-type="﻿Correlation analysis" id="SECID0EIKAE">
        <title>﻿Correlation analysis</title>
        <p>Based on the experimental data for the plant growth indices evaluated, correlation analysis for the bacterial and plant data sets was performed as described in the section Materials and Methods. The results are presented in Table <xref ref-type="table" rid="T2">2</xref>. They prove a positive relationship between the <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 and the growth parameters of the plant root system and the vigour index. In quantitative aspect, the correlation coefficient (<italic>r</italic>) can be evaluated as a very strong one since its values fall into the range 0.9–1.0 for the 16 h grown culture and 0.4–1.0 for the 48 h one.</p>
        <table-wrap id="T2" position="float" orientation="portrait">
          <label>Table 2.</label>
          <caption>
            <p>Correlation coefficients for the relationship <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Ps.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> and plant root system growth parameters.</p>
          </caption>
          <table id="TID0EOGAG" rules="all">
            <tbody>
              <tr>
                <th rowspan="1" colspan="1">Time (h) / Index</th>
                <th rowspan="1" colspan="1">Radicle</th>
                <th rowspan="1" colspan="1">Coleoptile</th>
                <th rowspan="1" colspan="1">Lateral roots</th>
                <th rowspan="1" colspan="1">Vigour index</th>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">16</td>
                <td rowspan="1" colspan="1">0,98927</td>
                <td rowspan="1" colspan="1">0,99982059</td>
                <td rowspan="1" colspan="1">0,95572399</td>
                <td rowspan="1" colspan="1">0,975104</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">48</td>
                <td rowspan="1" colspan="1">0,891681</td>
                <td rowspan="1" colspan="1">0,99194071</td>
                <td rowspan="1" colspan="1">0,36147266</td>
                <td rowspan="1" colspan="1">0,90716648</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec sec-type="﻿Pseudomonas putida 1046 PGP effect on soybean" id="SECID0EHNAE">
        <title>﻿<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 PGP effect on soybean</title>
        <p>In order to confirm the <abbrev xlink:title="plant growth-promoting" id="ABBRID0EZNAE">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain on the corn test plant, two different approaches were used: testing another plant model system and extended research on <abbrev xlink:title="plant growth-promoting" id="ABBRID0EIOAE">PGP</abbrev> characteristics of the bacterial strain.</p>
        <p>Soybean (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Glycine">Glycine</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="max">max</tp:taxon-name-part></tp:taxon-name></italic> L.) was exploited as a second model system. The crop has a global position as one of the most significant agri-cultures, a source of food, protein, and oil. The <abbrev xlink:title="plant growth-promoting" id="ABBRID0EZOAE">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 was evaluated using two of the indices applied for the corn: length of the radicle and the epicotile (coleoptile). The tendency for enhanced germination due to the increased number of lateral roots and enlarged epicotile length, promoted by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046, is confirmed by the data depicted in Fig. <xref ref-type="fig" rid="F4">4A, B</xref>.</p>
        <fig id="F4" position="float" orientation="portrait">
          <object-id content-type="arpha">843A6ACC-C122-5322-9395-5CDC173C4C81</object-id>
          <label>Figure 4.</label>
          <caption>
            <p><abbrev xlink:title="plant growth-promoting" id="ABBRID0E6PAE">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 on the germination of soybean seeds presented through the growth parameters length of radicle (<bold>A</bold>) and length of epicotile (<bold>B</bold>).</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g004.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849445.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849445</uri>
          </graphic>
        </fig>
        <p>The ability of the model bacterial strain to produce siderophores and solubilize phosphates was examined by qualitative analyses. These activities were tested due to their promotional effect on plant growth: enhanced metal accumulation in plants and putative application for phytoremediation purposes of siderophores, and the growth-promoting ability attributed to phosphate solubilization. The data about these <abbrev xlink:title="plant growth-promoting" id="ABBRID0EZQAE">PGP</abbrev> characteristics are presented in Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F6">6</xref>. They indicate the production of siderophores of hydroxamate type (hallo coloured in yellow-orange) and the typical colourless hallo of the solubilized phosphates.</p>
        <fig id="F5" position="float" orientation="portrait">
          <object-id content-type="arpha">818A950A-719F-5F6C-826C-D82F6B20710C</object-id>
          <label>Figure 5.</label>
          <caption>
            <p>Siderophore production by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046.</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g005.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849446.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849446</uri>
          </graphic>
        </fig>
        <fig id="F6" position="float" orientation="portrait">
          <object-id content-type="arpha">47DBD50A-3B2D-5365-9747-B21C3AFE30E0</object-id>
          <label>Figure 6.</label>
          <caption>
            <p>Phosphate solubilization activity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046.</p>
          </caption>
          <graphic xlink:href="biorisk-20-115_article-97581__-g006.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_849447.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/849447</uri>
          </graphic>
        </fig>
      </sec>
    </sec>
    <sec sec-type="﻿Discussion" id="SECID0EVSAE">
      <title>﻿Discussion</title>
      <p>Nowadays, extensive research is focused on <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0E2SAE">PGPR</abbrev> as a versatile replacement of fertilizers, pesticides, and other agrochemicals for the promotion of plant growth. <abbrev xlink:title="Plant Growth Promoting Rhizobacteria" id="ABBRID0E6SAE">PGPR</abbrev> influence in a positive way (directly or indirectly) the soil structure and fertility, decomposition of organic matter and organic pollutants, solubilization of nutrients of mineral nature, production of plant growth regulators, stimulation of the root growth, and execution of biocontrol against soil and seed-borne pathogens. (<xref ref-type="bibr" rid="B10">Gupta et al. 2015</xref>). Assessment of the plant growth-promoting potential of rhizobacteria requires a complex approach that includes, among others, the monitoring of plant germination capacity in test systems.</p>
      <p>The data presented in the Results section outline the positive effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain on the germination capacity of the technical crop <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Zea">Zea</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="mays">mays</tp:taxon-name-part></tp:taxon-name></italic>. Its biochemical profile speculated <abbrev xlink:title="plant growth-promoting" id="ABBRID0E6TAE">PGP</abbrev> potential, and the determined <abbrev xlink:title="plant growth-promoting" id="ABBRID0EDUAE">PGP</abbrev> traits confirmed it. The <italic>in vitro</italic> treatment of the model plants with bacterial strain improved their germination capacity. <xref ref-type="bibr" rid="B8">Gholami et al. (2009)</xref> reported similar results regarding improved seeds germination potential of corn. Other authors observed the same tendency for various crop cultures, such as canola (<xref ref-type="bibr" rid="B9">Glick et al. 1997</xref>), wheat (<xref ref-type="bibr" rid="B4">de Freitas and Germida 1992</xref>), sunflower (<xref ref-type="bibr" rid="B21">Shaukat et al. 2006</xref>), and potato (<xref ref-type="bibr" rid="B7">Frommel et al. 1993</xref>), where significant enhancement of the seeds’ emergence was registered – up to 100% of untreated control. It can be speculated that these findings are due to the activity of hydrolytic enzymes that assure intensive substrate assimilation (e.g., α-amylases for the starch) and promote early germination. The enhanced hormones biosynthesis might trigger the activity of these hydrolytic enzymes. In addition, hormone dependency seems to increase the vigour index due to promoted synthesis of indoleacetic acid, the most abundant representative of auxins family of phytohormones. Its role in the root initiation and elongation and in differentiation and proliferation of plant tissues has been well documented (<xref ref-type="bibr" rid="B15">Meliani et al. 2017</xref>). Our results with soybean additionally enlarged the spectrum of the crop cultures subjectable to the <abbrev xlink:title="plant growth-promoting" id="ABBRID0EBVAE">PGP</abbrev> effect of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic>.</p>
      <p>The physiological status of the culture is a parameter correlating with its biosynthetic capacity. The metabolically active 16 h culture expressed high values for the three tested indices and strong correlation coefficients of the bacterial and model plant data sets resulting in a better germination capacity. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> strains and plants are in commensal relationships. The root exudates of the plant feed the bacteria, and the bacteria stimulate plant growth through the production of hormone precursors and antibiotics that suppress the pathogens’ growth. It also supports nutrients immobilization (<xref ref-type="bibr" rid="B17">Molina et al. 2019</xref>). The data comparison for the 16 h and 48 h cultures indicated that the former executed its stimulatory function efficiently enough to result in high values for the all tested indices. The values for the length of the radicle and the coleoptile for the 0.2% suspension of the 48 h culture were slightly higher compared to those for the 16 h one (22.87% <italic>vs.</italic> 28.33%; and 35.96% <italic>vs.</italic> 45.96%). However, the shorter cultivation period (16 <italic>vs.</italic> 48 h) for the bacterial strain can compensate the difference of 5.5% to 10% since this is a defined technological advancement. Furthermore, the third index (the number of the lateral roots) is better presented in the 16 h compared to the 48 h bacterial culture (16.67% <italic>vs.</italic> 5.41). In fact, the formation of lateral roots contributes to the increase of the root surface reflecting the nutrients’ assimilation.</p>
    </sec>
    <sec sec-type="﻿Conclusions" id="SECID0EJWAE">
      <title>﻿Conclusions</title>
      <p>The results demonstrate that the <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain possesses defined plant growth-promoting capacity. It enhances the process of corn germination due to the increased number of lateral roots and enlarged length of the coleoptile and the root. The optimal treatment parameters of the corn seeds, considering both the physiological and economic aspects of the process, comprise the application of 0.2% suspension of 16 h grown <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain for five days.</p>
      <p>The positive germination capacity effect exerted by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain contributes to improve our knowledge of the variety of approaches and mechanisms that are implicated in the plant growth promotion by these bacteria. However, greater understanding of the interaction between bacteria and host plants requires further study. From an economic point of view, in light of the possible application of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudomonas">Pseudomonas</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="putida">putida</tp:taxon-name-part></tp:taxon-name></italic> 1046 strain as a bioinoculant, the use of less concentrated suspension is more feasible and cost-effective.</p>
    </sec>
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