Effects of overexpression of PKAc genes on expressions of lignin-modifying enzymes by Pleurotus ostreatus

References

• Kirk TK, Connors WJ, Bleam RD, et al. Preparation and microbial decomposition of synthetic [14C]ligins. Proc. Natl. Acad. Sci. USA. 1975;72:2515–2519.10.1073/pnas.72.7.2515
   PubMed Web of Science ®Google Scholar
• Floudas D, Binder M, Riley R, et al. The paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes. Science. 2012;336:1715–1719.10.1126/science.1221748
   PubMed Web of Science ®Google Scholar
• Cullen D, Kersten PJ. Enzymology and molecular biology of lignin degradation. In: Brambl R, Marzluf GA, editors. Biochemistry and molecular biology. vol. III. Springer-Verlag; 2004. p. 249–273.
   Google Scholar
• Dashtban M, Schraft H, Syed TA, et al. Fungal biodegradation and enzymatic modification of lignin. Int. J. Biochem. Mol. Biol. 2010;1:36–50.
   PubMedGoogle Scholar
• Hofrichter M, Ullrich R, Pecyna MJ, et al. New and classic families of secreted fungal heme peroxidases. Appl. Microbiol. Biotechnol. 2010;87:871–897.10.1007/s00253-010-2633-0
   PubMed Web of Science ®Google Scholar
• Heinzkill M, Messner K. The ligninolytic system of fungi. In: Anke T editor. Fungal biotechnology. Weinheim: Wiley-VCH; 1997. p. 213–227.
   Google Scholar
• Riley R, Salamov AA, Brown DW, et al. Extensive sampling of basidiomycete genomes demonstrates inadequacy of the white-rot/brown-rot paradigm for wood decay fungi. Proc. Natl. Acad. Sci. USA. 2014;111:9923–9928.10.1073/pnas.1400592111
   PubMed Web of Science ®Google Scholar
• Moreno AD, Ibarra D, Alvira P, et al. A review of biological delignification and detoxification methods for lignocellulosic bioethanol production. Crit. Rev. Biotechnol. 2014;10:10.
   Google Scholar
• Janusz G, Kucharzyk KH, Pawlik A, et al. Fungal laccase, manganese peroxidase and lignin peroxidase: gene expression and regulation. Enzyme Microb Technol. 2013;52:1–12.10.1016/j.enzmictec.2012.10.003
   PubMed Web of Science ®Google Scholar
• Salame TM, Knop D, Levinson D, et al. Release of Pleurotus ostreatus versatile-peroxidase from Mn2+ repression enhances anthropogenic and natural substrate degradation. PLoS One. 2012;7:e52446.10.1371/journal.pone.0052446
   Google Scholar
• Sugiura T, Mori T, Kamei I, et al. Improvement of ligninolytic properties in the hyper lignin-degrading fungus Phanerochaete sordida YK-624 using a novel gene promoter. FEMS Microbiol. Lett. 2012;331:81–88.10.1111/fml.2012.331.issue-1
   PubMed Web of Science ®Google Scholar
• Sakamoto T, Yao Y, Hida Y, et al. A calmodulin inhibitor, W-7 influences the effect of cyclic adenosine 3′, 5′-monophosphate signaling on ligninolytic enzyme gene expression in Phanerochaete chrysosporium. AMB Express. 2012;2:7.10.1186/2191-0855-2-7
   PubMed Web of Science ®Google Scholar
• MacDonald J, Suzuki H, Master ER. Expression and regulation of genes encoding lignocellulose-degrading activity in the genus Phanerochaete. Appl. Microbiol. Biotechnol. 2012;94:339–351.10.1007/s00253-012-3937-z
   PubMed Web of Science ®Google Scholar
• Singh D, Zeng J, Chen S. Increasing manganese peroxidase productivity of Phanerochaete chrysosporium by optimizing carbon sources and supplementing small molecules. Lett. Appl. Microbiol. 2011;53:120–123.10.1111/lam.2011.53.issue-1
   PubMed Web of Science ®Google Scholar
• Boominathan K, Reddy CA. cAMP-mediated differential regulation of lignin peroxidase and manganese-dependent peroxidase production in the white-rot basidiomycete Phanerochaete chrysosporium. Proc. Natl. Acad. Sci. USA. 1992;89:5586–5590.10.1073/pnas.89.12.5586
   PubMed Web of Science ®Google Scholar
• MacDonald MJ, Paterson A, Broda P. Possible relationship between cyclic AMP and idiophasic metabolism in the white rot fungus Phanerochaete chrysosporium. J. Bacteriol. 1984;160:470–472.
   PubMed Web of Science ®Google Scholar
• Fernández-Fueyo E, Ruiz-Dueñas FJ, Martínez MJ, et al. Ligninolytic peroxidase genes in the oyster mushroom genome: heterologous expression, molecular structure, catalytic and stability properties, and lignin-degrading ability. Biotechnol. Biofuels. 2014;7:2.10.1186/1754-6834-7-2
   PubMed Web of Science ®Google Scholar
• Fernández-Fueyo E, Castanera R, Ruiz-Duenas FJ, et al. Ligninolytic peroxidase gene expression by Pleurotus ostreatus: Differential regulation in lignocellulose medium and effect of temperature and pH. Fungal Genet. Biol. 2014;18:150–161.
   Web of Science ®Google Scholar
• Ruiz-Dueñas FJ, Fernández E, Martínez MJ, et al. Pleurotus ostreatus heme peroxidases: an in silico analysis from the genome sequence to the enzyme molecular structure. C R Biol. 2011;334:795–805.10.1016/j.crvi.2011.06.004
   PubMed Web of Science ®Google Scholar
• Yao Y, Sakamoto T, Honda Y, et al. The white-rot fungus Pleurotus ostreatus transformant overproduced intracellular cAMP and laccase. Biosci. Biotechnol. Biochem. 2013;77:2309–2311.10.1271/bbb.130470
   PubMed Web of Science ®Google Scholar
• Suetomi T, Sakamoto T, Tokunaga Y, et al. Effects of calmodulin on expression of lignin-modifying enzymes in Pleurotus ostreatus. Curr. Genet. 2014;61:127–140.
   PubMed Web of Science ®Google Scholar
• Dürrenberger F, Wong K, Kronstad JW. Identification of a cAMP-dependent protein kinase catalytic subunit required for virulence and morphogenesis in Ustilago maydis. Proc. Natl. Acad. Sci. USA. 1998;95:5684–5689.10.1073/pnas.95.10.5684
   PubMed Web of Science ®Google Scholar
• Salame TM, Knop D, Tal D, et al. Predominance of a versatile-peroxidase-encoding gene, mnp4, as demonstrated by gene replacement via a gene targeting system for Pleurotus ostreatus. Appl. Environ. Microbiol. 2012;78:5341–5352.10.1128/AEM.01234-12
   PubMed Web of Science ®Google Scholar
• Honda Y, Matsuyama T, Irie T, et al. Carboxin resistance transformation of the homobasidiomycete fungus Pleurotus ostreatus. Curr. Genet. 2000;37:209–212.10.1007/s002940050521
   PubMed Web of Science ®Google Scholar
• Salame TM, Yarden O, Hadar Y. Pleurotus ostreatus manganese-dependent peroxidase silencing impairs decolourization of Orange II. Microb. Biotechnol. 2010;3:93–106.10.1111/mbt.2010.3.issue-1
   PubMed Web of Science ®Google Scholar
• Dence CW. The determination of lignin. In: Lin SY, Dence CW, editors. Methods in lignin chemistry. Heidelberg: Springer-Verlag; 1992. p. 33–61.10.1007/978-3-642-74065-7
   Google Scholar
• Rowell RM, Pettersen R, Tshabalala MA. Cell wall chemistry. In: Rowell RM, editor. handbook of wood chemistry and wood composites. 2nd ed. New York, NY: CRC Press; 2013. p. 33–74.
   Google Scholar