Metabolic networks to generate pyruvate, PEP and ATP from glycerol in Pseudomonas fluorescens

被引:15
作者
Alhasawi, Azhar [1 ]
Thomas, Sean C. [1 ]
Appanna, Vasu D. [1 ]
机构
[1] Laurentian Univ, Fac Sci & Engn, Sudbury, ON P3E 2C6, Canada
关键词
Glycerol; Pyruvate; PEP; ATP; Metabolic networks; Bioconversion; Biodiesel; ANTIOXIDATIVE DEFENSE; BACILLUS-SUBTILIS; HYDROGEN-PEROXIDE; ADAPTATION; ALUMINUM; NADPH; OVEREXPRESSION; TOXICITY; COUNTERS; GALLIUM;
D O I
10.1016/j.enzmictec.2016.01.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glycerol is a major by-product of the biodiesel industry. In this study we report on the metabolic networks involved in its transformation into pyruvate, phosphoenolpyruvate (PEP) and ATP. When the nutritionally-versatile Pseudomonas fluorescens was exposed to hydrogen peroxide (H2O2) in a mineral medium with glycerol as the sole carbon source, the microbe reconfigured its metabolism to generate adenosine triphosphate (ATP) primarily via substrate-level phosphorylation (SLP). This alternative ATP-producing stratagem resulted in the synthesis of copious amounts of PEP and pyruvate. The production of these metabolites was mediated via the enhanced activities of such enzymes as pyruvate carboxylase (PC) and phosphoenolpyruvate carboxylase (PEPC). The high energy PEP was subsequently converted into ATP with the aid of pyruvate phosphate dikinase (PPDK), phosphoenolpyruvate synthase (PEPS) and pyruvate kinase (PK) with the concomitant formation of pyruvate. The participation of the phospho-transfer enzymes like adenylate kinase (AK) and acetate kinase (ACK) ensured the efficiency of this O-2-independent energy-generating machinery. The increased activity of glycerol dehydrogenase (GDH) in the stressed bacteria provided the necessary precursors to fuel this process. This H2O2-induced anaerobic life-style fortuitously evokes metabolic networks to an effective pathway that can be harnessed into the synthesis of ATP, PEP and pyruvate. The bioconversion of glycerol to pyruvate will offer interesting economic benefit. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:51 / 56
页数:6
相关论文
共 28 条
[1]   Aspartate metabolism and pyruvate homeostasis triggered by oxidative stress in Pseudomonas fluorescens: a functional metabolomic study [J].
Alhasawi, Azhar ;
Leblanc, Martine ;
Appanna, Nishma D. ;
Auger, Christopher ;
Appanna, Vasu D. .
METABOLOMICS, 2015, 11 (06) :1792-1801
[2]   Glycine metabolism and anti-oxidative defence mechanisms in Pseudomonas fluorescens [J].
Alhasawi, Azhar ;
Castonguay, Zachary ;
Appanna, Nishma D. ;
Auger, Christopher ;
Appanna, Vasu D. .
MICROBIOLOGICAL RESEARCH, 2015, 171 :26-31
[3]   A NOVEL ROLE FOR CALCITE IN CALCIUM HOMEOSTASIS [J].
ANDERSON, S ;
APPANNA, VD ;
HUANG, J ;
VISWANATHA, T .
FEBS LETTERS, 1992, 308 (01) :94-96
[4]   MANGANESE ELICITS THE SYNTHESIS OF A NOVEL EXOPOLYSACCHARIDE IN AN ARCTIC RHIZOBIUM [J].
APPANNA, VD ;
PRESTON, CM .
FEBS LETTERS, 1987, 215 (01) :79-82
[5]  
Auger C., 2014, BIOCHIM BIOPHYS ACTA, V1850, P43
[6]   A facile electrophoretic technique to monitor phosphoenolpyruvate-dependent kinases [J].
Auger, Christopher ;
Appanna, Varun ;
Castonguay, Zachary ;
Han, Sungwon ;
Appanna, Vasu D. .
ELECTROPHORESIS, 2012, 33 (07) :1095-1101
[7]   The Metabolic Reprogramming Evoked by Nitrosative Stress Triggers the Anaerobic Utilization of Citrate in Pseudomonas fluorescens [J].
Auger, Christopher ;
Lemire, Joseph ;
Cecchini, Dominic ;
Bignucolo, Adam ;
Appanna, Vasu D. .
PLOS ONE, 2011, 6 (12)
[8]   The overexpression of NADPH-producing enzymes counters the oxidative stress evoked by gallium, an iron mimetic [J].
Beriault, R. ;
Hamel, R. ;
Chenier, D. ;
Mailloux, Ryan J. ;
Joly, H. ;
Appanna, V. D. .
BIOMETALS, 2007, 20 (02) :165-176
[9]   Hydrogen peroxide stress provokes a metabolic reprogramming in Pseudomonas fluorescens: Enhanced production of pyruvate [J].
Bignucolo, Adam ;
Appanna, Varun P. ;
Thomas, Sean C. ;
Auger, Christopher ;
Han, Sungwon ;
Omri, Abdelwahab ;
Appanna, Vasu D. .
JOURNAL OF BIOTECHNOLOGY, 2013, 167 (03) :309-315
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3