| Literature DB >> 23871654 |
Adam Bignucolo1, Varun P Appanna, Sean C Thomas, Christopher Auger, Sungwon Han, Abdelwahab Omri, Vasu D Appanna.
Abstract
Pseudomonas fluorescens invoked a metabolic reconfiguration that resulted in enhanced production of pyruvate under the challenge of hydrogen peroxide (H₂O₂). Although this stress led to a sharp reduction in the activities of numerous tricarboxylic acid (TCA) cycle enzymes, there was a marked increase in the activities of catalase and various NADPH-generating enzymes to counter the oxidative burden. The upregulation of phosphoenolpyruvate synthase (PEPS) and pyruvate kinase (PK) coupled with the reduction of pyruvate dehydrogenase (PDH) in the H₂O₂-challenged cells appear to be important contributors to the elevated levels of pyruvate found in these bacteria. Increased pyruvate synthesis was evident in the presence of a variety of carbon sources including d-glucose. Intact cells rapidly consumed d-glucose with the concomitant formation of this monocarboxylic acid. At least a 12-fold increase in pyruvate production within 1h was observed in the stressed cells. These findings may be exploited in the development of technologies aimed at the conversion of carbohydrates into pyruvate.Entities:
Keywords: 6-phosphogluconate dehydrogenase; 6PGDH; BN-PAGE; BSA; Bioconversion; CFE; ETC; FUM; G6PDH; GDH; HPLC; ICDH; KGDH; Metabolic reconfiguration; NADPH-generating enzymes; PDH; PEPS; PK; Phosphoenolpyruvate synthase; Pyruvate production; TCA; alpha-ketoglutarate dehydrogenase; blue native polyacrylamide gel electrophoresis; bovine serum albumin; cell free extract; electron transport chain; fumarase; glucose-6-phosphate dehydrogenase; glutamate dehydrogenase; high performance liquid chromatography; isocitrate dehydrogenase; phosphoenolpyruvate synthase; pyruvate dehydrogenase; pyruvate kinase; tricarboxylic acid
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Year: 2013 PMID: 23871654 DOI: 10.1016/j.jbiotec.2013.07.002
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307