Accelerating glycolytic flux of Torulopsis glabrata CCTCC M202019 at high oxidoreduction potential created using potassium ferricyanide

Biotechnology Progress

Volumn 26, Issue 6, 2010, Pages 1551-1557

  Qin, Yi ^a   Liu, Li Ming ^a   Li, Chang Hao ^a   Xu, Sha ^a   Chen, Jian ^a  

^a JIANGNAN UNIVERSITY   (China)

Author keywords

Glycolytic flux; NADH; Oxidoreduction potential; Potassium ferricyanide; Torulopsis glabrata

Indexed keywords

GLYCOLYTIC FLUX; NADH; OXIDOREDUCTION POTENTIAL; POTASSIUM FERRICYANIDE; TORULOPSIS GLABRATA;

CATALYSTS; ENZYMES; GENE EXPRESSION; GLUCOSE; OXIDATION; PHOSPHORYLATION; POTASSIUM;

DISSOLVED OXYGEN;

FERRIC CITRATE IRON REDUCTASE; FERRICYANIDE; FLAVINE MONONUCLEOTIDE REDUCTASE; NICOTINAMIDE ADENINE DINUCLEOTIDE; OXYGEN; POTASSIUM FERRICYANIDE;

ARTICLE; CANDIDA GLABRATA; CHEMISTRY; GLYCOLYSIS; METABOLISM; OXIDATION REDUCTION REACTION; PHOSPHORYLATION;

CANDIDA GLABRATA; FERRICYANIDES; FMN REDUCTASE; GLYCOLYSIS; NAD; OXIDATION-REDUCTION; OXYGEN; PHOSPHORYLATION;

CANDIDA GLABRATA;

EID: 78650189962     PISSN: 87567938     EISSN: 15206033     Source Type: Journal    
DOI: 10.1002/btpr.496     Document Type: Article

References (47)

1. Moreno-Sanchez R, Saavedra E, Rodriguez-Enriquez S, Olin-Sandoval V. Metabolic control analysis: a tool for designing strategies to manipulate metabolic pathways. J Biomed Biotechnol. 2008; 2008: 597913.
2. Larsson C, Nilsson A, Blomberg A, Gustafsson L. Glycolytic flux is conditionally correlated with ATP concentration in Saccharomyces cerevisiae: a chemostat study under carbon- or nitrogen-limiting conditions. J Bacteriol. 1997; 179: 7243-7250.
3. Zhu Y, Eiteman, MA, Altman, R, Altman E. High glycolytic flux improves pyruvate production by a metabolically engineered Escherichia coli strain. Appl Environ Microbiol. 2008; 74: 6649-6655.
4. Vemuri GN, Eiteman MA, McEwen JE, Olsson L, Nielsen J. Increasing NADH oxidation reduces overflow metabolism in Saccharomyces cerevisiae. Proc Natl Acad Sci USA. 2007; 104: 2402-2407.
5. Garrigues C, Loubiere P, Lindley ND, Cocaign-Bousquet M. Control of the shift from homolactic acid to mixed-acid fermentation in Lactococcus lactis: predominant role of the NADH/NAD+ ratio. J Bacteriol. 1997; 179: 5282-5287.
6. Even S, Garrigues C, Loubiere P, Lindley ND, Cocaign-Bousquet M. Pyruvate metabolism in Lactococcus lactis is dependent upon glyceraldehyde-3-phosphate dehydrogenase activity. Metab Eng. 1999; 1: 198-205.
7. Alberti KG. The biochemical consequences of hypoxia. J Clin Pathol Suppl (R Coll Pathol). 1977; 11: 14-20.
8. Heuser F, Schroer K, Lutz S, Bringer-Meyer S, Sahm H. Enhancement of the NAD(P)(H) pool in Escherichia coli for biotransformation. Eng Life Sci. 2007; 7: 343-353.
9. Berrios-Rivera SJ, San KY, Bennett GN. The effect of NAPRTase overexpression on the total levels of NAD, the NADH/NAD(+) ratio, and the distribution of metabolites in Escherichia coli. Metab Eng. 2002; 4: 238-247.
10. Geertman JMA, van Maris AJA, van Dijken JP, Pronk JT. Physiological and genetic engineering of cytosolic redox metabolism in Saccharomyces cerevisiae for improved glycerol production. Metab Eng. 2006; 8: 532-542.
11. Zhang YP, Li Y, Du CY, Liu M, Cao Z. Inactivation of aldehyde dehydrogenase: a key factor for engineering 1, 3-propanediol production by Klebsiella pneumoniae. Metab Eng. 2006; 8: 578-586.
12. Zhang Y, Huang Z, Du C, Li Y, Cao Z. Introduction of an NADH regeneration system into Klebsiella oxytoca leads to an enhanced oxidative and reductive metabolism of glycerol. Metab Eng. 2009; 11: 101-106.
13. Hou J, Lages NF, Oldiges M, Vemuri GN. Metabolic impact of redox cofactor perturbations in Saccharomyces cerevisiae. Metab Eng. 2009; 11: 253-261.
14. + availability. J Biotechnol. 2006; 126: 173-185.
15. de Graef MR, Alexeeva S, Snoep JL, Teixeira de Mattos MJ. The steady-state internal redox state (NADH/NAD) reflects the external redox state and is correlated with catabolic adaptation in Escherichia coli. J Bacteriol. 1999; 181: 2351-2357.
16. Lin H, Bennett GN, San KY. Effect of carbon sources differing in oxidation state and transport route on succinate production in metabolically engineered Escherichia coli. J Ind Microbiol Biotechnol. 2005; 32: 87-93.
17. Qiang H, Shimuzu K. Effect of dissolved oxygen concentration on the intracellular flux distribution for pyruvate fermentation. J Biotechnol. 1999; 68: 135-147.
18. Du CY, Yan H, Zhang YP, Li Y, Cao ZA. Use of oxidoreduction potential as an indicator to regulate 1, 3-propanediol fermentation by Klebsiella pneumoniae. Appl Microbiol Biotechnol. 2006; 69: 554-563.
19. Husson F, Tu VP, Santiago-Gomez M, Cachon R, Feron G, Nicaud JM, Kermasha S, Belin JM. Effect of redox potential on the growth of Yarrowia lipolytica and the biosynthesis and activity of heterologous hydroperoxide lyase. J Mol Catal B: Enzym. 2006; 39: 179-183.
20. Feron G, Mauvais G, Lherminier J, Michel J, Wang XD, Viel C, Cachon R. Metabolism of fatty acid in yeast: addition of reducing agents to the reaction medium influences P-oxidation activities, gamma-decalactone production, and cell ultrastructure in Sporidiobolus ruinenii cultivated on ricinoleic acid methyl ester. Can J Microbiol. 2007; 53: 738-749.
21. Riondet C, Cachon R, Wache Y, Alcaraz G, Divies C. Extracellular oxidoreduction potential modifies carbon and electron flow in Escherichia coli. J Bacteriol. 2000; 182: 620-626.
22. Gill RT, Cha HJ, Jain A, Rao G, Bentley WE. Generating controlled reducing environments in aerobic recombinant Escherichia coli fermentations: effects on cell growth, oxygen uptake, heat shock protein expression, and in vivo CAT activity. Biotechnol Bioeng. 1998; 59: 248-259.
23. Berovic M. Scale-up of citric acid fermentation by redox potential control. Biotechnol Bioeng. 1999; 64: 552-557.
24. Kastner JR, Eiteman MA, Lee SA. Effect of redox potential on stationary-phase xylitol fermentations using Candida tropicalis. Appl Microbiol Biotechnol. 2003; 63: 96-100.
25. Kieronczyk A, Cachon R, Feron G, Yvon M. Addition of oxidizing or reducing agents to the reaction medium influences amino acid conversion to aroma compounds by Lactococcus lactis. J Appl Microbiol. 2006; 101: 1114-1122.
26. Atsumi S, Hanai T, Liao JC. Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels. Nature. 2008; 451: 86-89.
27. Causey TB, Shanmugam KT, Yomano LP, Ingram LO. Engineering Escherichia coli for efficient conversion of glucose to pyruvate. Proc Natl Acad Sci USA. 2004; 101: 2235-2240.
28. Wang Q, He P, Lu D, Shen A, Jiang N. Screening of pyruvate-producing yeast and effect of nutritional conditions on pyruvate production. Lett Appl Microbiol. 2002; 35: 338-342.
29. Bernofsky C, Swan M. An improved cycling assay for nicotinamide adenine dinucleotide. Anal Biochem. 1973; 53: 452-458.
30. Leonardo MR, Cunningham PR, Clark DP. Anaerobic regulation of the adhE gene, encoding the fermentative alcohol dehydrogenase of Escherichia coli. J Bacteriol. 1993; 175: 870-878.
31. Liu L, Li Y, Li H, Chen J. Significant increase of glycolytic flux in Torulopsis glabrata by inhibition of oxidative phosphorylation. FEMS Yeast Res. 2006; 6: 1117-1129.
32. Moreira dos Santos M, Raghevendran V, Kotter P, Olsson L, Nielsen J. Manipulation of malic enzyme in Saccharomyces cerevisiae for increasing NADPH production capacity aerobically in different cellular compartments. Metab Eng. 2004; 6: 352-363.
33. Zhang J, Snyder SH. Nitric oxide stimulates auto-ADP-ribosylation of glyceraldehyde-3-phosphate dehydrogenase. Proc Natl Acad Sci USA. 1992; 89: 9382-9385.
34. Valadi A, Granath K, Gustafsson L, Adler L. Distinct intracellular localization of Gpd1p and Gpd2p, the two yeast isoforms of NAD(+)-dependent glycerol-3-phosphate dehydrogenase, explains their different contributions to redox-driven glycerol production. J Biol Chem. 2004; 279: 39677-39685.
35. Postma E, Verduyn C, Scheffers WA, Van Dijken JP. Enzymic analysis of the crabtree effect in glucose-limited chemostat cultures of Saccharomyces cerevisiae. Appl Environ Microbiol. 1989; 55: 468-477.
36. Viegas CA, Sebastiao PB, Nunes AG, Sa-Correia I. Activation of plasma membrane H(+)-ATPase and expression of PMA1 and PMA2 genes in Saccharomyces cerevisiae cells grown at supraoptimal temperatures. Appl Environ Microbiol. 1995; 61: 1904-1909.
37. Deneer HG, Healey V, Boychuk I. Reduction of exogenous ferric iron by a surface-associated ferric reductase of Listeria spp. Microbiology. 1995; 141: 1985-1992.
38. Klassen R, Fricke J, Pfeiffer A, Meinhardt F. A modified DNA isolation protocol for obtaining pure RT-PCR grade RNA. Biotechnol Lett. 2008; 30: 1041-1044.
39. Muller H, Hennequin C, Gallaud J, Dujon B, Fairhead C. The asexual yeast Candida glabrata maintains distinct a and alpha haploid mating types. Eukaryot Cell. 2008; 7: 848-858.
40. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-Delta Delta C) method. Methods. 2001; 25: 402-408.
41. Zhou J, Huang L, Liu L, Chen J. Enhancement of pyruvate productivity by inducible expression of a F(0)F(1)-ATPase inhibitor INH1 in Torulopsis glabrata CCTCC M202019. J Biotechnol. 2009; 144: 120-126.
42. Larsson C, Pahlman IL, Gustafsson L. The importance of ATP as a regulator of glycolytic flux in Saccharomyces cerevisiae. Yeast. 2000; 16: 797-809.
43. Clark MG, Partick EJ, Patten GS, Crane FL, Low H, Grebing C. Evidence for the extracellular reduction of ferricyanide by rat liver. A trans-plasma membrane redox system. Biochem J. 1981; 200: 565-572.
44. Askerlund P, Laurent P, Nakagawa H, Kader JC. NADH-ferricyanide reductase of leaf plasma membranes partial purification and immunological relation to potato tuber microsomal NADH-ferricyanide reductase and spinach leaf NADH-nitrate reductase. Plant Physiol. 1991; 95: 6-13.
45. Fischer E, Strehlow B, Hartz D, Braun V. Soluble and membrane-bound ferrisiderophore reductases of Escherichia coli K-12. Arch Microbiol. 1990; 153: 329-336.
46. Morrissey JA, Williams PH, Cashmore AM. Candida albicans has a cell-associated ferric-reductase activity which is regulated in response to levels of iron and copper. Microbiology. 1996; 142 (Part 3): 485-492.
47. Dancis A, Klausner RD, Hinnebusch AG, Barriocanal JG. Genetic evidence that ferric reductase is required for iron uptake in Saccharomyces cerevisiae. Mol Cell Biol. 1990; 10: 2294-2301.