Gene expression and function involved in polyol biosynthesis of Trichosporonoides megachiliensis under hyper-osmotic stress

Journal of Bioscience and Bioengineering

Volumn 115, Issue 6, 2013, Pages 645-650

  Kobayashi, Yosuke ^a   Yoshida, Junjiro ^a   Iwata, Hisashi ^a   Koyama, Yoshiyuki ^a   Kato, Jun ^a   Ogihara, Jun ^a   Kasumi, Takafumi ^a  

^a NIHON UNIVERSITY   (Japan)

Author keywords

Er1; Er2; Er3; Erythritol; Erythrose reductase; Gcy1; Glycerol; Gpd1; Osmotic stress; Trichosporonoides megachiliensis

Indexed keywords

ER1; ER2; ER3; ERYTHRITOL; ERYTHROSE REDUCTASE; GCY1; GPD1; OSMOTIC STRESS; TRICHOSPORONOIDES MEGACHILIENSIS;

BIOCHEMISTRY; BIOSYNTHESIS; ENZYME ACTIVITY; GLYCEROL; METABOLISM; OSMOSIS; YEAST;

GENE EXPRESSION;

ER1 PROTEIN; ER2 PROTEIN; ER3 PROTEIN; ERBIUM; ERYTHRITOL; GLYCEROL; GLYCEROL 3 PHOSPHATE DEHYDROGENASE; UNCLASSIFIED DRUG;

ARTICLE; AUREOBASIDIUM; CONTROLLED STUDY; FUNGAL STRAIN; GENE AMPLIFICATION; GENE EXPRESSION; GENE FUNCTION; GENE SEQUENCE; HYPEROSMOTIC STRESS; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN SYNTHESIS; SACCHAROMYCES CEREVISIAE; SEQUENCE ANALYSIS; SOLUTE; START CODON; TRICHOSPORONOIDES MEGACHILIENSIS;

ALDEHYDE REDUCTASE; BASIDIOMYCOTA; ERYTHRITOL; FUNGAL PROTEINS; GENE EXPRESSION; GLYCEROL; OSMOTIC PRESSURE; POLYMERS; SACCHAROMYCES CEREVISIAE;

SACCHAROMYCES CEREVISIAE; TRICHOSPORONOIDES MEGACHILIENSIS;

EID: 84877004821     PISSN: 13891723     EISSN: 13474421     Source Type: Journal    
DOI: 10.1016/j.jbiosc.2012.12.004     Document Type: Article

References (27)

1. Ishizuka H., Wako K., Kasumi T., Sasaki T. Breeding of a mutant of Aureobasidium sp. with high erythritol production. J. Ferment. Bioeng. 1989, 68:310-314.
2. Rosa C.A., Jindamorakot S., Limtong S., Nakase T., Lachance M.A., Fidalgo-Jiméne A., Daniel H.M., Pagnocca F.C., Inácio J., Morais P.B. Synonymy of the yeast genera Moniliella and Trichosporonoides and proposal of Moniliella fonsecae sp. nov. and five new species combinations. Int. J. Syst. Evol. Microbiol. 2009, 59:425-429.
3. Wako K., Kawaguchi G., Kubo N., Kasumi T., Hayashi K. Newly isolated yeasts producing high yields of polyols. Hakkokogaku 1988, 66:209-215.
4. Hohmann S. Osmotic stress signaling and osmoadaptation in yeasts. Microbiol. Mol. Biol. Rev. 2002, 66:300-372.
5. Noda K., Oku T. Metabolism and disposition of erythritol after oral administration to rats. J. Nutr. 1992, 122:1266-1272.
6. Lina B.A., Bos-Kuijpers M.H., Til H.P., Bär A. Chronic toxicity and carcinogenicity study of erythritol in rats. Regul. Toxicol. Pharmacol. 1996, 24:S264-S279.
7. den Hartog G.J., Boots A.W., Adam-Perrot A., Brouns F., Verkooijen I.W., Weseler A.R., Haenen G.R., Bast A. Erythritol is a sweet antioxidant. Nutrition 2010, 26:449-458.
8. Sawada K., Taki A., Takashi Y., Seki M. Key role for transketolase activity in erythritol production by Trichosporonoides megachiliensis SN-G42. J. Biosci. Bioeng. 2009, 108:385-390.
9. Richter H., Vlad D., Unden G. Significance of pantothenate for glucose fermentation by Oenococcus oeni and for suppression of the erythritol and acetate production. Arch. Microbiol. 2001, 175:26-31.
10. Ishizuka H., Tokuoka K., Sasaki T., Taniguchi H. Purification and some properties of an Erythrose Reductase from an Aureobasidium sp. mutant. Biosci. Biotechnol. Biochem. 1992, 56:941-945.
11. Ookura T., Azuma K., Isshiki K., Taniguchi H., Kasumi T., Kawamura Y. Primary structure analysis and functional expression of erythrose reductases from erythritol-producing fungi (Trichosporonoides megachiliensis SNG-42). Biosci. Biotechnol. Biochem. 2005, 69:944-951.
12. Hur E., Wilson D.K. The crystal structure of the GCY1 protein from S. cerevisiae suggests a divergent aldo-keto reductase catalytic mechanism. Chem. Biol. Interact. 2001, 130-132:527-536.
13. Magdolen V., Oechsner U., Trommler P., Bandlow W. Transcriptional control by galactose of a yeast gene encoding a protein homologous to mammalian aldo/keto reductases. Gene 1990, 90:105-114.
14. Norbeck J., Blomberg A. Metabolic and regulatory changes associated with growth of Saccharomyces cerevisiae in 1.4 M NaCl. Evidence for osmotic induction of glycerol dissimilation via the dihydroxyacetone pathway. J. Biol. Chem. 1997, 272:5544-5554.
15. Chang Q., Griest T.A., Harter T.M., Petrash J.M. Functional studies of aldo-keto reductases in Saccharomyces cerevisiae. Biochim. Biophys. Acta 2007, 1773:321-329.
16. Yoshida J., Kobayashi Y., Tanaka Y., Koyama Y., Kato J., Ogihara J., Shima J., Kasumi T. Complementary function of mitogen-activated protein kinase Hog1 from Trichosporonoides megachiliensis in Saccharomyces cerevisiae under hyper-osmotic stress. J. Biosci. Bioeng. 2013, 115:127-132.
17. Inoue H., Nojima H., Okayama H. High efficiency transformation of Escherichia coli with plasmids. Gene 1990, 96:23-28.
18. Ito H., Fukuda Y., Murata K., Kimura A. Transformation of intact yeast cells treated with alkali cations. J. Bacteriol. 1983, 153:163-168.
19. Clotet J., Posas F. Control of cell cycle in response to osmostress lessons from yeast. Methods Enzymol. 2007, 428:63-76.
20. Sharma P., Meena N., Aggarwal M., Mondal A.K. Debaryomyces hansenii, a highly osmo-tolerant and halo-tolerant yeast, maintains activated Dhog1p in the cytoplasm during its growth under severe osmotic stress. Curr. Genet. 2005, 48:162-170.
21. Proft M., Mas G., de Nadal E., Vendrell A., Noriega N., Struhl K., Posas F. The stress-activated Hog1 kinase is a selective transcriptional elongation factor for genes responding to osmotic stress. Mol. Cell 2006, 23:241-250.
22. Alepuz P.M., Jovanovic A., Reiser V., Ammerer G. Stress-induced MAP kinase Hog1 is part of transcription activation complexes. Mol. Cell 2001, 7:767-777.
23. Moskvina E., Schüller C., Maurer C.T., Mager W.H., Ruis H. A search in the genome of Saccharomyces cerevisiae for genes regulated via stress response elements. Yeast 1998, 14:1041-1050.
24. Kaino T., Takagi H. Gene expression profiles and intracellular contents of stress protectants in Saccharomyces cerevisiae under ethanol and sorbitol stresses. Appl. Microbiol. Biotechnol. 2008, 79:273-283.
25. Kayingo G., Wong B. The MAP kinase Hog1p differentially regulates stress-induced production and accumulation of glycerol and d-arabitol in Candida albicans. Microbiology 2005, 151:2987-2999.
26. Tekolo O.M., McKenzie J., Botha A., Prior B.A. The osmotic stress tolerance of basidiomycetous yeasts. FEMS Yeast Res. 2010, 10:482-491.
27. Lee J.K., Kim S.Y., Ryu Y.W., Seo J.H., Kim J.H. Purification and characterization of a novel erythrose reductase from Candida magnoliae. Appl. Environ. Microbiol. 2003, 69:3710-3718.