4.4 Article

Optimization of Direct Lysine Decarboxylase Biotransformation for Cadaverine Production with Whole-Cell Biocatalysts at High Lysine Concentration

Journal

JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume 25, Issue 7, Pages 1108-1113

Publisher

KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
DOI: 10.4014/jmb.1412.12052

Keywords

Biotransformation; whole-cell biocatalyst; lysine decarboxylase; cadaverine; high-concentration reaction; Escherichia coli

Funding

  1. MOTIE/KEIT [10047910]
  2. National Research Foundation of Korea - Ministry of Education [NRF-2013R1A1A2A10004690, NRF-2011-619-E0002]
  3. Korea Ministry of Environment through Converging Technology Project [2012-000620001]
  4. Korea Environmental Industry & Technology Institute (KEITI) [ARQ201206081003] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [10047910] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2013R1A1A2A10004690] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Cadaverine (1,5-diaminopentane) is an important industrial chemical with a wide range of applications. Although there have been many efforts to produce cadaverine through fermentation, there are not many reports of the direct cadaverine production from lysine using biotransformation. Whole-cell reactions were examined using a recombinant Escherichia coli strain overexpressing the E. coli MG1655 cadA gene, and various parameters were investigated for the whole-cell bioconversion of lysine to cadaverine. A high concentration of lysine resulted in the synthesis of pyridoxa1-5'-phosphate (PLP) and it was found to be a critical control factor for the biotransformation of lysine to cadaverine. When 0.025 mM PLP and 1.75 M lysine in 500 mM sodium acetate buffer (pH6) were used, consumption of 91% lysine and conversion of about 80% lysine to cadaverine were successfully achieved.

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