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  <title><![CDATA[Phd Defense by   Luz Karime Medina Cordoba]]></title>
  <body><![CDATA[<p>&nbsp;</p>

<p>In partial fulfillment of the requirements for the degree of&nbsp;</p>

<p>&nbsp;</p>

<p>Doctor of Philosophy in Biology</p>

<p>in the&nbsp;</p>

<p>School of Biological Sciences</p>

<p>&nbsp;</p>

<p><strong>Luz Karime Medina Cordoba</strong></p>

<p>&nbsp;</p>

<p>will defend her dissertation</p>

<p>&nbsp;</p>

<p><strong>Biofertilizers for Sustainable Agriculture: Isolation and Genomic Characterization of Nitrogen-Fixing Bacteria from Sugarcane</strong></p>

<p>&nbsp;</p>

<p>Tuesday, December 10, 2019</p>

<p>1:00 PM</p>

<p>Klaus&nbsp;Advanced Computing Building</p>

<p>Conference Room&nbsp;1116 East&nbsp;</p>

<p>&nbsp;</p>

<p><strong>Thesis Advisor:</strong></p>

<p>Dr. Joel E. Kostka</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p><strong>Co-Advisor:</strong></p>

<p>Dr. I. King Jordan</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p><strong>Committee Members:</strong></p>

<p>Dr. Frank Stewart</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p>Dr. Jung H. Choi</p>

<p>School of Biological Sciences</p>

<p>Georgia Institute of Technology</p>

<p>&nbsp;</p>

<p>Dr. Leonard W. Mayer</p>

<p>School of Medicine</p>

<p>Emory University&nbsp;</p>

<p>&nbsp;</p>

<p><strong>Abstract</strong></p>

<p>The goal of my thesis research was to explore the use of bacterial biofertilizers, as an alternative or complementary approach to chemical fertilizers, in support of more sustainable agricultural practices.&nbsp; To this end, I worked to discover and characterize native nitrogen-fixing bacteria that are associated with sugarcane crops cultivated in the Cauca Valley of Colombia.&nbsp; I hypothesized that native nitrogen-fixing bacteria, found in association with local sugarcane crops could serve as potent biofertilizers with the potential to simultaneously increase crop yield while reducing the reliance on chemical fertilizers.&nbsp; I evaluated this hypothesis by isolating nitrogen-fixing bacteria isolated from Colombian sugarcane fields and characterizing their plant growth-promoting (PGP) potential using an integrated computational genomics and experimental approach.&nbsp;</p>

<p>A high-throughput cultivation approach was developed and applied for the enrichment and isolation of nitrogen-fixing bacteria from environmental samples.&nbsp; Pure cultures of nitrogen-fixing bacteria were isolated and tested for diazotrophic potential by PCR amplification of <em>nifH</em> genes, a common molecular marker for nitrogen-fixing capacity, and twenty-two distinct <em>nifH</em> positive isolates were selected for genome sequencing and analysis.&nbsp; Genome sequence analysis confirmed the presence of intact <em>nifH&nbsp;</em>genes and operons in the genomes of 18 of the isolates, and isolate genomes were found to encode operons for phosphate solubilization, siderophore production, and other PGP phenotypes.&nbsp; I characterized 14 of the 22 nitrogen-fixing isolates as distinct strains of <em>Klebsiella pneumoniae</em>, and four others were members of genera that are closely related to <em>Klebsiella</em>.&nbsp;</p>

<p>Computational phenotype predictions for PGP traits were validated with a series of experimental laboratory assays for nitrogen fixation and phosphate solubilization as well as the production of siderophores, gibberellic acid, and indole acetic acid.&nbsp; Results from the biochemical assays were consistent with the bioinformatic predictions for these isolates, in support of their PGP potential.&nbsp; The quantitative approach to computational phenotyping that I developed and applied to sugarcane bacterial isolates facilitates the screening for strains that have a high potential for nitrogen fixation and other PGP phenotypes while showing minimal risk for virulence and antibiotic resistance.&nbsp;</p>

<p>Finally, I developed and validated an automated method to curate and continuously update a <em>nifH </em>reference sequence database, which can be used to support the characterization of metagenomic or environmental amplicon sequences.&nbsp; This process yields a far smaller, but much more reliable, set of &lsquo;gold-standard&rsquo; <em>nifH</em> sequences, against which users can compare their metagenomic or amplicon sequence data for accurate functional prediction and taxonomic characterization of environmental samples.</p>

<p>&nbsp;</p>

<p>&nbsp;</p>
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