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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2017-03-25</publicationDate>
    
        <volume>14</volume>
        <issue>1</issue>

 
    <startPage>415</startPage>
    <endPage>419</endPage>

	 
      <doi>10.13005/bbra/2460</doi>
        <publisherRecordId>22999</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Biotin Axotroph Mutants of Native Corynebacterium Glutamicum for the Fermentative Production of L-Glutamic Acid</title>

    <authors>
	 


      <author>
       <name>V. Krishnarjuna Reddy</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>U. Keerthi</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name> A. V. N. Swamy</name>

		
	<affiliationId>2</affiliationId>
      </author>
    

	 


      <author>
       <name>Dowlathabad Muralidhara Rao</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biotechnology, Sri Krishnadevaraya University, Ananthapuramu, India.</affiliationName>
    

		
		<affiliationName affiliationId="2">Department of Chemical Engineering, Jawaharlal Nehru Technological University Ananthapuram, Ananthapuramu, India.</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng"><p style="text-align: left;">The present paper deals with isolation of <em>C.glutamicum</em> strain and strain improvement of <em>C.glutamicum</em> by mutation studies for the production of L-Glutamic acid. Native isolate of <em>C.glutamicum</em>was manipulated to excrete L-glutamate. The modified protocol was used in this paper to trigger L-glutamate excretion. The important feature of this protocol is to achieve a biotin concentration that is low enough to activate glutamate excretion but high adequate to still allow sufficient growth of the cells. To achieve this appropriate biotin concentration, a pre cultivation step is required in order to deplete the cells of biotin. Later Physical Mutation was induced on Biotin depleted <em>C.glutamicum</em> strain.</p></abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol14no1/biotin-axotroph-mutants-of-native-corynebacterium-glutamicum-for-the-fermentative-production-of-l-glutamic-acid/</fullTextUrl>



      <keywords language="eng">
        <keyword><p style="text-align: left;"><em>Biotin;Corynebacterium glutamicum: Fermentation </em>L-Glutamic acid;</p></keyword>
      </keywords>

  </record>
</records>