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Biotransformation of phenol to glutamate by Corynebacterium glutamicum
                                      ATCC 13032: molecular and biochemical studies

                                           1 B Jaya Bhargavi*,  B Muralidhara Rao
                                                            1

                   1 Department of Biotechnology, Sri Krishnadeveraya University, Anantapuram-515003, India.

               Corresponding author: bargaviphd@gmail.com

               Abstract:

               The present study aimed to investigate the biotransformation of phenol to glutamate by C. glutamicum
               using  molecular  and  biochemical  studies.  At  the  molecular  level,  the  effect  of  phenol  on  mRNA
               expression levels of genes associated with phenol degradation pathway [transcriptional regulator AraC
               family  member  pheR,  phenol  hydroxylase  (phe),  catechol  1,2-dioxygenase  (catA)],  TCA  cycle  [2-
               oxoglutarate  dehydrogenase  (odhA)],  glutamate  synthesis  [glutamate  dehydrogenase  (gdh)],  stress
               response [dihydrolipoamide dehydrogenase (lpd) and L-transpeptidase (lpps)], fatty acid synthesis [beta
               subunit of homolog of acetyl CoA carboxylase or detergent sensitivity rescuer (dtsR1)] and regulator
               of 2-oxoglutarate dehydrogenase [serine/threonine protein kinase (pknG)] in C. glutamicum grown on
               phenol medium under two experimental conditions: 200 ppm phenol plus 1% yeast extract and 300 ppm
               phenol plus 1.1% yeast extract was investigated. The results indicated that significant up-regulation of
               pheR, phe, catA, lpps, lpd and gdh is associated with significant down-regulation of odhA, dtsR1 and
               pknG was observed in C. glutamicum grown on phenol medium over bacteria grown on yeast extract
               alone. Further, biochemical studies indicated that the activity levels of 2-oxoglutarate dehydrogenase
               were significantly reduced, while significant elevation in the activity levels of glutamate dehydrogenase
               was observed in cell-free extracts of C. glutamicum grown on phenol medium over controls. The results
               also indicated that the  C. glutamicum utilize phenol as carbon and energy source thereby promote
               glutamate synthesis as evidenced by a significant increase in the glutamate levels in the medium. To
               conclude, environmental pollution caused by phenol is of major concern and to mitigate the phenol
               toxicity,  eco-friendly  approaches  are  needed.  The  current  study  highlights  the  phenol  degradation
               potential of C. glutamicum and its transformation to glutamate. The results were discussed in the light
               of literature.

               Keywords: C. glutamicum, Growth, Glutamate, Phenol yeast extract
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