Oxidative stress in industrial fungi

References

• Abrashev R, Dolashka P, Christova R, Stefanova L, Angelova M. 2005. Role of antioxidant enzymes in survival of conidiospores of Aspergillus niger 26 under conditions of temperature stress. J Appl Microbiol 99(4): 902–909.
   PubMedGoogle Scholar
• Abrashev RI, Pashova SB, Stefanova LN, Vassilev SV, Dolashka-Angelova PA, Angelova MB. 2008. Heat-shock-induced oxidative stress and antioxidant response in Aspergillus niger 26. Can J Microbiol 54(12): 977–983.
   PubMedGoogle Scholar
• Alvarez-Peral FJ, Zaragoza O, Pedreno Y, Arguelles JC. 2002. Protective role of trehalose during severe oxidative stress caused by hydrogen peroxide and the adaptive oxidative stress response in Candida albicans. Microbiology 148(8): 2599–2606.
   PubMedGoogle Scholar
• Ames BN, Shigenaga MK, Hagen TM. 1995. Mitochondrial decay in aging. Biochim Biophys Acta 1271(1): 165–170.
   PubMedGoogle Scholar
• Angelova MB, Pashova SB, Spasova BK, Vassilev SV, Slokoska LS. 2005. Oxidative stress response of filamentous fungi induced by hydrogen peroxide and paraquat. Mycol Res 109(2): 150–158.
   PubMedGoogle Scholar
• Arguelles JC. 2000. Physiological roles of trehalose in bacteria and yeasts: a comparative analysis. Arch Microbiol 174(4): 217–224.
   PubMedGoogle Scholar
• Bai Z, Harvey LM, McNeil B. 2001. Use of the chemiluminescent probe lucigenin to monitor the production of the superoxide anion radical in a recombinant Aspergillus niger B1-D. Biotechnol Bioeng 75(2): 204–211.
   PubMedGoogle Scholar
• Bai Z, Harvey LM, McNeil B. 2003a. Elevated temperature effects on the oxidant/antioxidant balance in submerged batch cultures of the filamentous fungus Aspergillus niger B1-D. Biotechnol Bioeng 83(7): 772–779.
   PubMedGoogle Scholar
• Bai Z, Harvey LM, McNeil B. 2003b. Oxidative stress in submerged cultures of fungi. Crit Rev Biotechnol 23(4): 267–302.
   PubMedGoogle Scholar
• Bai Z, Harvey LM, McNeil B. 2003c. Physiological responses of chemostat cultures of Aspergillus niger B1-D to simulated and actual oxidative stress. Biotechnol Bioeng 82(6): 691–701.
   PubMedGoogle Scholar
• Bai Z, Harvey LM, White S, McNeil B. 2004. Effects of oxidative stress on production of heterologous and native protein, and culture morphology in batch and chemostat cultures of Aspergillus niger B1-D. Enzyme Microb Technol 34(1): 10–21.
   Google Scholar
• Beckman JS, Koppenol WH. 1996. Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. Am J Physiol 271: C1424–1437.
   PubMed Web of Science ®Google Scholar
• Beinert H, Holm RH, Munck E. 1997. Iron-sulfur clusters: nature’s modular, multipurpose structures. Science 277(5326): 653–659.
   PubMedGoogle Scholar
• Benaroudj N, Lee DH, Goldberg AL. 2001. Trehalose accumulation during cellular stress protects cells and cellular proteins from damage by oxygen radicals. J Biol Chem 276(26): 24261–24267.
   PubMedGoogle Scholar
• Benov L, Fridovich I. 1995. Superoxide dismutase protects against aerobic heat shock in Escherichia coli. J Bacteriol 177(11): 3344–3346.
   PubMedGoogle Scholar
• Bilinski T, Krawiec Z, Liczmanski A, Litwinska J. 1985. Is hydroxyl radical generated by the Fenton reaction in vivo? Biochem Biophys Res Commun 130(2): 533–539.
   PubMedGoogle Scholar
• Bussink HJ, Oliver R. 2001. Identification of two highly divergent catalase genes in the fungal tomato pathogen, Cladosporium fulvum. Eur J Biochem 268(1): 15–24.
   PubMedGoogle Scholar
• Cabiscol E, Piulats E, Echave P, Herrero E, Ros J. 2000. Oxidative stress promotes specific protein damage in Saccharomyces cerevisiae. J Biol Chem 275(35): 27393–27398.
   PubMedGoogle Scholar
• Cadenas E, Davies KJ. 2000. Mitochondrial free radical generation, oxidative stress, and aging. Free Radic Biol Med 29(3-4): 222–230.
   PubMedGoogle Scholar
• Carneiro P, Duarte M, Videira A. 2004. The main external alternative NAD(P)H dehydrogenase of Neurospora crassa mitochondria. Biochim Biophys Acta 1608(1): 45–52.
   PubMedGoogle Scholar
• Chance B, Sies H, Boveris A. 1979. Hydroperoxide metabolism in mammalian organs. Physiol Rev 59(3): 527–605.
   PubMed Web of Science ®Google Scholar
• Chen Q, Thorpe J, Dohmen JR, Li F, Keller JN. 2006. Ump1 extends yeast lifespan and enhances viability during oxidative stress: central role for the proteasome? Free Radic Biol Med 40(1): 120–126.
   PubMedGoogle Scholar
• Colussi C, Albertini MC, Coppola S, Rovidati S, Galli F, Ghibelli L. 2000. H2O2-induced block of glycolysis as an active ADP-ribosylation reaction protecting cells from apoptosis. FASEB J 14(14): 2266–2276.
   PubMedGoogle Scholar
• Costa VM, Amorim MA, Quintanilha A, Moradas-Ferreira P. 2002. Hydrogen peroxide-induced carbonylation of key metabolic enzymes in Saccharomyces cerevisiae: the involvement of the oxidative stress response regulators Yap1 and Skn7. Free Radic Biol Med 33(11): 1507–1515.
   PubMedGoogle Scholar
• Culotta VC, Yang M, O’Halloran TV 2006. Activation of superoxide dismutases: putting the metal to the pedal. Biochim Biophys Acta 1763(7): 747–758.
   PubMedGoogle Scholar
• Dalle-Donne I, Rossi R, Giustarini D, Milzani A, Colombo R. 2003. Protein carbonyl groups as biomarkers of oxidative stress. Clin Chim Acta 329(1-2): 23–38.
   PubMedGoogle Scholar
• Dalton TP, Shertzer HG, Puga A. 1999. Regulation of gene expression by reactive oxygen. Annu Rev Pharmacol Toxicol 39: 67–101.
   PubMed Web of Science ®Google Scholar
• Davidson JF, Schiestl RH. 2001a. Cytotoxic and genotoxic consequences of heat stress are dependent on the presence of oxygen in Saccharomyces cerevisiae. J Bacteriol 183(15): 4580–4587.
   PubMedGoogle Scholar
• Davidson JF, Schiestl RH. 2001b. Mitochondrial respiratory electron carriers are involved in oxidative stress during heat stress in Saccharomyces cerevisiae. Mol Cell Biol 21(24): 8483–8489.
   PubMedGoogle Scholar
• Davidson JF, Whyte B, Bissinger PH, Schiestl RH. 1996. Oxidative stress is involved in heat-induced cell death in Saccharomyces cerevisiae. Proc Natl Acad Sci USA 93(10): 5116–5121.
   PubMedGoogle Scholar
• Davies KJ. 2001. Degradation of oxidized proteins by the 20S proteasome. Biochimie 83(3-4): 301–310.
   PubMedGoogle Scholar
• Davies KJ, Lin SW. 1988a. Degradation of oxidatively denatured proteins in Escherichia coli. Free Radic Biol Med 5(4): 215–223.
   PubMedGoogle Scholar
• Davies KJ, Lin SW. 1988b. Oxidatively denatured proteins are degraded by an ATP-independent proteolytic pathway in Escherichia coli. Free Radic Biol Med 5(4): 225–236.
   PubMedGoogle Scholar
• Denicola A, Batthyany C, Lissi E, Freeman BA, Rubbo H, Radi R. 2002. Diffusion of nitric oxide into low density lipoprotein. J Biol Chem 277(2): 932–936.
   PubMedGoogle Scholar
• Dikalov S, Jiang J, Mason RP. 2005. Characterization of the high-resolution ESR spectra of superoxide radical adducts of 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide (DEPMPO) and 5,5-dimethyl-1-pyrroline N-oxide (DMPO). Analysis of conformational exchange. Free Radic Res 39(8): 825–836.
   PubMedGoogle Scholar
• Emri T, Pocsi I, Szentirmai A. 1997. Glutathione metabolism and protection against oxidative stress caused by peroxides in Penicillium chrysogenum. Free Radic Biol Med 23(5): 809–814.
   PubMedGoogle Scholar
• Emri T, Pocsi I, Szentirmai A. 1999. Analysis of the oxidative stress response of Penicillium chrysogenum to menadione. Free Radic Res 30(2): 125–132.
   PubMedGoogle Scholar
• Fernandes DC, Wosniak J Jr, Pescatore LA, Bertoline MA, Liberman M, Laurindo FR, Santos CX. 2007. Analysis of DHE-derived oxidation products by HPLC in the assessment of superoxide production and NADPH oxidase activity in vascular systems. Am J Physiol Cell Physiol 292(1): C413–422.
   Google Scholar
• Fillinger S, Chaveroche MK, van Dijck P, de Vries R, Ruijter G, Thevelein J, d’Enfert C. 2001. Trehalose is required for the acquisition of tolerance to a variety of stresses in the filamentous fungus Aspergillus nidulans. Microbiology 147(7): 1851–1862.
   PubMedGoogle Scholar
• Flint DH, Tuminello JF, Emptage MH. 1993. The inactivation of Fe-S cluster containing hydro-lyases by superoxide. J Biol Chem 268(30): 22369–22376.
   PubMedGoogle Scholar
• Fridovich I. 1995. Superoxide radical and superoxide dismutases. Annu Rev Biochem 64: 97–112.
   PubMed Web of Science ®Google Scholar
• Gardner PR, Fridovich I. 1991. Superoxide sensitivity of the Escherichia coli aconitase. J Biol Chem 266(29): 19328–19333.
   PubMedGoogle Scholar
• Gibbs PA, Seviour RJ, Schmid F. 2000. Growth of filamentous fungi in submerged culture: problems and possible solutions. Crit Rev Biotechnol 20(1): 17–48.
   PubMedGoogle Scholar
• Giulivi C, Boveris A, Cadenas E. 1995. Hydroxyl radical generation during mitochondrial electron transfer and the formation of 8-hydroxydeoxyguanosine in mitochondrial DNA. Arch Biochem Biophys 316(2): 909–916.
   PubMedGoogle Scholar
• Godon C, Lagniel G, Lee J, Buhler JM, Kieffer S, Perrot M, Boucherie H, Toledano MB, Labarre J. 1998. The H2O2 stimulon in Saccharomyces cerevisiae. J Biol Chem 273(35): 22480–22489.
   PubMedGoogle Scholar
• Gonzalez-Parraga P, Hernandez JA, Arguelles JC. 2003. Role of antioxidant enzymatic defences against oxidative stress H2O2 and the acquisition of oxidative tolerance in Candida albicans. Yeast 20(14): 1161–1169.
   PubMedGoogle Scholar
• Gralla EB, Kosman DJ. 1992. Molecular genetics of superoxide dismutases in yeasts and related fungi. Adv Genet 30: 251–319.
   PubMed Web of Science ®Google Scholar
• Grant CM, Collinson LP, Roe JH, Dawes IW. 1996. Yeast glutathione reductase is required for protection against oxidative stress and is a target gene for yAP-1 transcriptional regulation. Mol Microbiol 21(1): 171–179.
   PubMedGoogle Scholar
• Grant CM, Quinn KA, Dawes IW. 1999. Differential protein S-thiolation of glyceraldehyde-3-phosphate dehydrogenase isoenzymes influences sensitivity to oxidative stress. Mol Cell Biol 19(4): 2650–2656.
   PubMedGoogle Scholar
• Greenacre SA, Ischiropoulos H. 2001. Tyrosine nitration: localisation, quantification, consequences for protein function and signal transduction. Free Radic Res 34(6): 541–581.
   PubMedGoogle Scholar
• Grune T, Merker K, Sandig G, Davies KJ. 2003. Selective degradation of oxidatively modified protein substrates by the proteasome. Biochem Biophys Res Commun 305(3): 709–718.
   PubMedGoogle Scholar
• Halliwell B, Gutteridge JMC. 2007. Free Radicals in Biology and Medicine. Oxford, UK: Oxford University Press.
   Google Scholar
• Halliwell B, Whiteman M. 2004. Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean? Br J Pharmacol 142(2): 231–255.
   PubMedGoogle Scholar
• Hauptmann N, Grimsby J, Shih JC, Cadenas E. 1996. The metabolism of tyramine by monoamine oxidase A/B causes oxidative damage to mitochondrial DNA. Arch Biochem Biophys 335(2): 295–304.
   PubMedGoogle Scholar
• Hisada H, Hata Y, Kawato A, Abe Y, Akita O. 2005. Cloning and expression analysis of two catalase genes from Aspergillus oryzae. J Biosci Bioeng 99(6): 562–568.
   PubMedGoogle Scholar
• Imlay JA. 1995. A metabolic enzyme that rapidly produces superoxide, fumarate reductase of Escherichia coli. J Biol Chem 270(34): 19767–19777.
   PubMedGoogle Scholar
• Imlay JA, Fridovich I. 1991. Assay of metabolic superoxide production in Escherichia coli. J Biol Chem 266(11): 6957–6965.
   PubMedGoogle Scholar
• Inai Y, Nishikimi M. 2002. Increased degradation of oxidized proteins in yeast defective in 26S proteasome assembly. Arch Biochem Biophys 404(2): 279–284.
   PubMedGoogle Scholar
• Ingledew WM. 1999. Alcohol production by Saccharomyces cerevisiae. In: Jacques K, Lyons TP, Kelsall DR, eds. The Alcohol Textbook (pp. 71–72 ). 3rd ed. Nottingham, UK: Nottingham University Press.
   Google Scholar
• Inoue Y, Matsuda T, Sugiyama K, Izawa S, Kimura A. 1999. Genetic analysis of glutathione peroxidase in oxidative stress response of Saccharomyces cerevisiae. J Biol Chem 274(38): 27002–27009.
   PubMedGoogle Scholar
• Izawa S, Inoue Y, Kimura A. 1995. Oxidative stress response in yeast: effect of glutathione on adaptation to hydrogen peroxide stress in Saccharomyces cerevisiae. FEBS Lett 368(1): 73–76.
   PubMedGoogle Scholar
• Izawa S, Maeda K, Miki T, Mano J, Inoue Y, Kimura A. 1998. Importance of glucose-6-phosphate dehydrogenase in the adaptive response to hydrogen peroxide in Saccharomyces cerevisiae. Biochem J 330(2): 811–817.
   PubMedGoogle Scholar
• Jackson SK, Liu KJ, Liu M, Timmins GS. 2002. Detection and removal of contaminating hydroxylamines from the spin trap DEPMPO, and re-evaluation of its use to indicate nitrone radical cation formation and S(N)1 reactions. Free Radic Biol Med 32(3): 228–232.
   PubMedGoogle Scholar
• James WO, Elliot DC. 1995. Cyanide-resistant mitochondria from the spadix of an Arum. Nature (175): 89.
   PubMedGoogle Scholar
• Jamieson DJ. 1992. Saccharomyces cerevisiae has distinct adaptive responses to both hydrogen peroxide and menadione. J Bacteriol 174(20): 6678–6681.
   PubMedGoogle Scholar
• Jamieson DJ, Rivers SL, Stephen DW. 1994. Analysis of Saccharomyces cerevisiae proteins induced by peroxide and superoxide stress. Microbiology 140(12): 3277–3283.
   PubMedGoogle Scholar
• Jamieson DJ, Stephen DW, Terriere EC. 1996. Analysis of the adaptive oxidative stress response of Candida albicans. FEMS Microbiol Lett 138(1): 83–88.
   PubMedGoogle Scholar
• Joseph-Horne T, Hollomon DW, Wood PM. 2000. Fungal respiration: a fusion of standard and alternative components. Biochim Biophys Acta 1504: 179–195.
   Google Scholar
• Juhnke H, Krems B, Kotter P, Entian KD. 1996. Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress. Mol Gen Genet 252(4): 456–464.
   PubMedGoogle Scholar
• Karaffa L, Vaczy K, Sandor E, Biro S, Szentirmai A, Pocsi I. 2001. Cyanide-resistant alternative respiration is strictly correlated to intracellular peroxide levels in Acremonium chrysogenum. Free Radic Res 34(4): 405–416.
   PubMedGoogle Scholar
• Kawasaki L, Aguirre J. 2001. Multiple catalase genes are differentially regulated in Aspergillus nidulans. J Bacteriol 183(4): 1434–1440.
   PubMedGoogle Scholar
• Kawasaki L, Wysong D, Diamond R, Aguirre J. 1997. Two divergent catalase genes are differentially regulated during Aspergillus nidulans development and oxidative stress. J Bacteriol 179(10): 3284–3292.
   PubMedGoogle Scholar
• Kelsall KT, Lyons TP. (1999). Management of fermentations in the production of alcohol: moving towards 23% ethanol. In: Jacques K, Lyons TP, Kelsall DR, eds. The Alcohol Textbook (pp. 27–33 ). 3rd ed. Nottingham, UK: Nottingham University Press.
   Google Scholar
• Kirimura K, Yoda M, Shimizu H, Sugano S, Mizuno M, Kino K, Usami S. 2000. Contribution of cyanide-insensitive respiratory pathway, catalyzed by the alternative oxidase, to citric acid production in Aspergillus niger. Biosci Biotechnol Biochem 64(10): 2034–2039.
   PubMedGoogle Scholar
• Kreiner M, McNeil B, Harvey LM. 2000. “Oxidative stress” response in submerged cultures of a recombinant Aspergillus niger B1-D. Biotechnol Bioeng 70(6): 662–669.
   PubMedGoogle Scholar
• Kreiner M, Harvey LM, McNeil B. 2002. Oxidative stress response of a recombinant Aspergillus niger to exogenous menadione and H2O2 addition. Enzyme Microb Technol 30(3): 346–353.
   Google Scholar
• Kreiner M, Harvey LM, McNeil B. 2003. Morphological and enzymatic responses of a recombinant Aspergillus niger to oxidative stressors in chemostat cultures. J Biotechnol 100(3): 251–260.
   PubMedGoogle Scholar
• Krumova E, Dolashki A, Pashova S, Dolashka-Angelova P, Stevanovic S, Hristova R, Stefanova L, Voelter W, Angelova M. 2008. Unusual location and characterization of Cu/Zn-containing superoxide dismutase from filamentous fungus Humicola lutea. Arch Microbiol 189(2): 121–130.
   PubMedGoogle Scholar
• Lee J-S, Hah Y-C, Roe J-H. 1993. The induction of oxidative enzymes in Streptomyces coelicolor upon hydrogen peroxide treatment. J Gen Microbiol 139: 1013–1018.
   Google Scholar
• Lee JC, Straffon MJ, Jang TY, Higgins VJ, Grant CM, Dawes IW. 2001. The essential and ancillary role of glutathione in Saccharomyces cerevisiae analysed using a grande gsh1 disruptant strain. FEMS Yeast Res 1(1): 57–65.
   PubMedGoogle Scholar
• Li Q, Abrashev R, Harvey LM, McNeil B. 2008a. Oxidative stress-associated impairment of glucose and ammonia metabolism in the filamentous fungus, Aspergillus niger B1-D. Mycol Res 112(9): 1049–1055.
   PubMedGoogle Scholar
• Li Q, Harvey LM, McNeil B. 2008b. The effects of elevated process temperature on the protein carbonyls in the filamentous fungus, Aspergillus niger B1-D. Proc Biochem 43(8): 877.
   Google Scholar
• Li Q, Harvey LM, McNeil B. 2008c. Oxygen enrichment effects on protein oxidation, proteolytic activity and the energy status of submerged batch cultures of Aspergillus niger B1-D. Proc Biochem 43(3): 238.
   Google Scholar
• Li Q, McNeil B, Harvey LM. 2008d. Adaptive response to oxidative stress in the filamentous fungus Aspergillus niger B1-D. Free Radic Biol Med 44(3): 394–402.
   PubMedGoogle Scholar
• Liochev SI, Fridovich I. 1998. Lucigenin as mediator of superoxide production: revisited. Free Radic Biol Med 25(8): 926–928.
   PubMedGoogle Scholar
• Longo VD, Liou LL, Valentine JS, Gralla EB. 1999. Mitochondrial superoxide decreases yeast survival in stationary phase. Arch Biochem Biophys 365(1): 131–142.
   PubMedGoogle Scholar
• Luo Y, Li WM, Wang W. 2008. Trehalose: protector of antioxidant enzymes or reactive oxygen species scavenger under heat stress? Environ Exp Bot 63(1-3): 378–384.
   Google Scholar
• Michan S, Lledias F, Baldwin JD, Natvig DO, Hansberg W. 2002. Regulation and oxidation of two large monofunctional catalases. Free Radic Biol Med 33(4): 521–532.
   PubMedGoogle Scholar
• Minagawa N, Koga S, Nakano M, Sakajo S, Yoshimoto A. 1992. Possible involvement of superoxide anion in the induction of cyanide-resistant respiration in Hansenula anomala. FEBS Lett 302(3): 217–219.
   PubMedGoogle Scholar
• Minard KI, McAlister-Henn L. 2001. Antioxidant function of cytosolic sources of NADPH in yeast. Free Radic Biol Med 31(6): 832–843.
   PubMedGoogle Scholar
• Moore AL, Bonner WD Jr, Rich PR. 1978. The determination of the proton-motive force during cyanide-insensitive respiration in plant mitochondria. Arch Biochem Biophys 186: 298–306.
   PubMedGoogle Scholar
• Naqui A, Chance B, Cadenas E. 1986. Reactive oxygen intermediates in biochemistry. Annu Rev Biochem 55: 137–166.
   PubMed Web of Science ®Google Scholar
• Navarro RE, Aguirre J. 1998. Posttranscriptional control mediates cell type-specific localization of catalase A during Aspergillus nidulans development. J Bacteriol 180(21): 5733–5738.
   PubMedGoogle Scholar
• Navarro RE, Stringer MA, Hansberg W, Timberlake WE, Aguirre J. 1996. catA, a new Aspergillus nidulans gene encoding a developmentally regulated catalase. Curr Genet 29(4): 352–359.
   PubMedGoogle Scholar
• Nedeva TS, Petrova VY, Zamfirova DR, Stephanova EV, Kujumdzieva AV. 2004. Cu/Zn superoxide dismutase in yeast mitochondria—a general phenomenon. FEMS Microbiol Lett 230(1): 19–25.
   PubMedGoogle Scholar
• Nienow AW. 1990. Agitators for mycelial fermentations. Trends Biotechnol 8: 224–233.
   Web of Science ®Google Scholar
• Noventa-Jordao MA, Couto RM, Goldman MH, Aguirre J, Iyer S, Caplan A, Terenzi HF, Goldman GH. 1999. Catalase activity is necessary for heat-shock recovery in Aspergillus nidulans germlings. Microbiology 145(11): 3229–3234.
   PubMedGoogle Scholar
• Nystrom T. 2005. Role of oxidative carbonylation in protein quality control and senescence. EMBO J 24(7): 1311–1317.
   PubMedGoogle Scholar
• O’Brien KM, Dirmeier R, Engle M, Poyton RO. 2004. Mitochondrial protein oxidation in yeast mutants lacking manganese-(MnSOD) or copper- and zinc-containing superoxide dismutase (CuZnSOD): evidence that MnSOD and CuZnSOD have both unique and overlapping functions in protecting mitochondrial proteins from oxidative damage. J Biol Chem 279(50): 51817–51827.
   PubMedGoogle Scholar
• O’Donnell A, Bai Y, Bai Z, McNeil B, Harvey LM. 2007. Introduction to bioreactors of shake-flask inocula leads to development of oxidative stress in Aspergillus niger. Biotechnol Lett 29(6): 895–900.
   PubMedGoogle Scholar
• Pedreno Y, Gimeno-Alcaniz JV, Matallana E, Arguelles JC. 2002. Response to oxidative stress caused by H2O2 in Saccharomyces cerevisiae mutants deficient in trehalase genes. Arch Microbiol 177(6): 494–499.
   PubMedGoogle Scholar
• Peraza L, Hansberg W. 2002. Neurospora crassa catalases, singlet oxygen and cell differentiation. Biol Chem 383(3-4): 569–575.
   PubMedGoogle Scholar
• Privalle CT, Fridovich I. 1987. Induction of superoxide dismutase in Escherichia coli by heat shock. Proc Natl Acad Sci USA 84(9): 2723–2726.
   PubMedGoogle Scholar
• Raitt DC, Johnson AL, Erkine AM, Makino K, Morgan B, Gross DS, Johnston LH. 2000. The Skn7 response regulator of Saccharomyces cerevisiae interacts with Hsf1 in vivo and is required for the induction of heat shock genes by oxidative stress. Mol Biol Cell 11(7): 2335–2347.
   PubMedGoogle Scholar
• Reinheckel T, Sitte N, Ullrich O, Kuckelkorn U, Davies KJ, Grune T. 1998. Comparative resistance of the 20S and 26S proteasome to oxidative stress. Biochem J 335(3): 637–642.
   PubMedGoogle Scholar
• Rich PR. 1978. Quinol oxidation in Arum maculatum mitochondria and its application to the assay, solubilisation and partial purification of the alternative oxidase. FEBS Lett 96: 252–256.
   Google Scholar
• Richter C. 1987. Biophysical consequences of lipid peroxidation in membranes. Chem Phys Lipids 44(2-4): 175–189.
   PubMedGoogle Scholar
• Schliebs W, Wurtz C, Kunau WH, Veenhuis M, Rottensteiner H. 2006. A eukaryote without catalase-containing microbodies: Neurospora crassa exhibits a unique cellular distribution of its four catalases. Eukaryot Cell 5(9): 1490–1502.
   PubMedGoogle Scholar
• Shanmuganathan A, Avery SV, Willetts SA, Houghton JE. 2004. Copper-induced oxidative stress in Saccharomyces cerevisiae targets enzymes of the glycolytic pathway. FEBS Lett 556(1-3): 253–259.
   PubMedGoogle Scholar
• Shenton D, Grant CM. 2003. Protein S-thiolation targets glycolysis and protein synthesis in response to oxidative stress in the yeast Saccharomyces cerevisiae. Biochem J 374(2): 513–519.
   PubMedGoogle Scholar
• Siedow JN, Umbach AL. 1995. Plant mitochondrial electron transfer and molecular biology. Plant Cell 7: 821–831.
   PubMedGoogle Scholar
• Sierra-Campos E, Valdez-Solana MA, Matuz-Mares D, Velazquez I, Pardo JP. 2009. Induction of morphological changes in Ustilago maydis cells by octyl gallate. Microbiology 155(2): 604–611.
   PubMedGoogle Scholar
• Steels EL, Learmonth RP, Watson K. 1994. Stress tolerance and membrane lipid unsaturation in Saccharomyces cerevisiae grown aerobically or anaerobically. Microbiology 140 (3): 569–576.
   PubMedGoogle Scholar
• Stephen DW, Jamieson DJ. 1996. Glutathione is an important antioxidant molecule in the yeast Saccharomyces cerevisiae. FEMS Microbiol Lett 141(2-3): 207–212.
   PubMedGoogle Scholar
• Sturtz LA, Diekert K, Jensen LT, Lill R, Culotta VC. 2001. A fraction of yeast Cu,Zn-superoxide dismutase and its metallochaperone, CCS, localize to the intermembrane space of mitochondria. A physiological role for SOD1 in guarding against mitochondrial oxidative damage. J Biol Chem 276(41): 38084–38089.
   PubMedGoogle Scholar
• Takasuka T, Sayers NM, Anderson MJ, Benbow EW, Denning DW. 1999. Aspergillus fumigatus catalases: cloning of an Aspergillus nidulans catalase B homologue and evidence for at least three catalases. FEMS Immunol Med Microbiol 23(2): 125–133.
   PubMedGoogle Scholar
• Tanaka T, Izawa S, Inoue Y. 2005. GPX2, encoding a phospholipid hydroperoxide glutathione peroxidase homologue, codes for an atypical 2-Cys peroxiredoxin in Saccharomyces cerevisiae. J Biol Chem 280(51): 42078–42087.
   PubMedGoogle Scholar
• Thieringer R, Kunau WH. 1991. The beta-oxidation system in catalase-free microbodies of the filamentous fungus Neurospora crassa. Purification of a multifunctional protein possessing 2-enoyl-CoA hydratase, L-3-hydroxyacyl-CoA dehydrogenase, and 3-hydroxyacyl-CoA epimerase activities. J Biol Chem 266(20): 13110–13117.
   PubMedGoogle Scholar
• Tian Y, Mao L, Okajima T, Ohsaka T. 2002. Superoxide dismutase-based third-generation biosensor for superoxide anion. Anal Chem 74(10): 2428–2434.
   PubMedGoogle Scholar
• Turrens JF. 2003. Mitochondrial formation of reactive oxygen species. J Physiol 552(2): 335–344.
   PubMedGoogle Scholar
• Valenciano S, Lucas JR, Pedregosa A, Monistrol IF, Laborda F. 1996. Induction of beta-oxidation enzymes and microbody proliferation in Aspergillus nidulans. Arch Microbiol 166(5): 336–341.
   PubMedGoogle Scholar
• Veiga A, Arrabaca JD, Loureiro-Dias MC. 2003. Stress situations induce cyanide-resistant respiration in spoilage yeasts. J Appl Microbiol 95(2): 364–371.
   PubMedGoogle Scholar
• Walker GM. 1998. Yeast Physiology and Biotechnology (pp. 20–21 ). Wiley, New Jersey, USA.
   Google Scholar
• Wallace MA, Liou LL, Martins J, Clement MH, Bailey S, Longo VD, Valentine JS, Gralla EB. 2004. Superoxide inhibits 4Fe-4S cluster enzymes involved in amino acid biosynthesis. Cross-compartment protection by CuZn-superoxide dismutase. J Biol Chem 279(31): 32055–32062.
   PubMedGoogle Scholar
• Wieser R, Adam G, Wagner A, Schuller C, Marchler G, Ruis H, Krawiec Z, Bilinski T. 1991. Heat shock factor-independent heat control of transcription of the CTT1 gene encoding the cytosolic catalase T of Saccharomyces cerevisiae. J Biol Chem 266(19): 12406–12411.
   PubMedGoogle Scholar
• Wojtaszek P. 1997. Oxidative burst: an early plant response to pathogen infection. Biochem J 322 (3): 681–692.
   PubMedGoogle Scholar
• Wong CM, Siu KL, Jin DY. 2004. Peroxiredoxin-null yeast cells are hypersensitive to oxidative stress and are genomically unstable. J Biol Chem 279(22): 23207–23213.
   PubMedGoogle Scholar
• Wongwicharn A, McNeil B, Harvey LM. 1999. Effect of oxygen enrichment on morphology, growth, and heterologous protein production in chemostat cultures of Aspergillus niger B1-D. Biotechnol Bioeng 65(4): 416–424.
   PubMedGoogle Scholar
• Yamada K, Nakagawa CW, Mutoh N. 1999. Schizosaccharomyces pombe homologue of glutathione peroxidase, which does not contain selenocysteine, is induced by several stresses and works as an antioxidant. Yeast 15(11): 1125–1132.
   PubMedGoogle Scholar
• Yukioka H, Inagaki S, Tanaka R, Katoh K, Miki N, Mizutani A, Masuko M. 1998. Transcriptional activation of the alternative oxidase gene of the fungus Magnaporthe grisea by a respiratory-inhibiting fungicide and hydrogen peroxide. Biochim Biophys Acta 1442(2-3): 161–169.
   PubMedGoogle Scholar