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Penicillium canescens Host as the Platform for Development of a New Recombinant Strain Producers of Carbohydrases

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Book cover Microorganisms in Biorefineries

Part of the book series: Microbiology Monographs ((MICROMONO,volume 26))

Abstract

The filamentous fungi strain Penicillium canescens has been developed as a host for the production of heterologous proteins and enzymes for biorefinery. There are several features of this strain which make it an attractive option as a host expression system. First, P. canescens has a high growth rate and the developed system of biosynthesis of extracellular enzymes; second, strain needs inexpensive fermentation medium using sugar beet pulp as a main substrate; third, the fermentation process can be easily scaled up; and fourth, there is auxotrophic strain P. canescens which can be transformed by plasmid DNA with exogenous genes. All these factors make possible to create new efficient recombinant strains and enzyme preparations (different endo-glucanases and cellobiohydrolases, β-glucosidase, pectin lyase, inulinases) that are in demand by various sectors of industry and biorefinery.

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References

  • Aleksenko AY, Makarova NA, Nikolaev IV (1995) Integrative and replicative transformation of Penicillium canescens with a heterologous nitrate-reductase gene. Curr Genet 28:474–477

    Article  CAS  PubMed  Google Scholar 

  • Aslanidis C, de Jong PJ (1990) Ligation-independent cloning of PCR products (LIC-PCR). Nucleic Acids Res 18:6069–6074

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Banerjee G, Car S, Scott-Craig JS, Borrusch MS, Walton JD (2010a) Rapid optimization of enzyme mixtures for deconstruction of diverse pretreatment/biomass feedstock combinations. Biotechnol Biofuels 3:22

    Article  PubMed Central  PubMed  Google Scholar 

  • Banerjee G, Car S, Scott-Craig JS, Borrusch MS, Bongers M, Walton JD (2010b) Synthetic multi-component enzyme mixtures for deconstruction of lignocellulosic biomass. Bioresour Technol 101:9097–9105

    Article  CAS  PubMed  Google Scholar 

  • Bushina EV (2012) New highly effective enzyme preparations for hydrolysis of the pectin- and cellulose containing substrates based on Penicillium canescens recombinant strains. Dissertation, Moscow State University

    Google Scholar 

  • Bushina EV, Rozhkova AM et al (2012) Development of complex enzymatic preparations of pactinases and cellulases for sugar beet marc digestion. Appl Biochem Microbiol (Russia) 48(5):543–549

    CAS  Google Scholar 

  • Gusakov AV, Sinitsyn AP, Berlin AG, Markov AV, Ankudimova NV (2000) Surface hydrophobic amino acid residues in cellulase molecules as a structural factor responsible for their high denim-washing performance. Enzyme Microb Technol 27:664–671

    Article  CAS  PubMed  Google Scholar 

  • Keranen KM, Pentilla M (1995) Production of recombinant proteins in the filamentous fungus Trichoderma reesei. Curr Opin Biotechnol 6(5):534–537

    Article  CAS  PubMed  Google Scholar 

  • Kumar R, Singh S, Singh OV (2008) Bioconversion of lignocellulosic biomass: biochemical and molecular perspectives. J Ind Microbiol Biotechnol 35(5):377–391

    Article  CAS  PubMed  Google Scholar 

  • Lubertoz D, Keasling JD (2009) Development Aspergillus as a host for heterologous expression. Biotechnol Adv 27(1):57–75

    Google Scholar 

  • Mach RL, Zeilinger S (2003) Regulation of gene expression in industrial fungi: Trichoderma. Appl Microbiol Biotechnol 60:515–522

    Article  CAS  PubMed  Google Scholar 

  • Nevalainen KM, Te’o VS, Bergquist PL (2005) Heterologous protein expression in filamentous fungi. Trends Biotechnol 23(9):468–474

    Article  CAS  PubMed  Google Scholar 

  • Nikolaev IV, Vinetski YP (1998) Arabinose induces synthesis of secreted β-galactosidase in the filamentous fungus Penicillium canescens. Biochemistry (Mosc) 63:1294–1298

    CAS  Google Scholar 

  • Nikolaev IV, Bekker OB, Serebryanyi VA, Chulkin AM, Vinetski YP (1999) The superproduction of secreted β-galactosidase by filamentous fungus Penicillium canescens: the structure of the gene and design of the multicopy producer. Biotechnology (Russ) 3:3–13

    Google Scholar 

  • Ochman H, Gerber AS, Hartl DL (1988) Genetic applications of an inverse polymerase chain reaction. Genetics 120:621

    CAS  PubMed Central  PubMed  Google Scholar 

  • Patent RU 2080387, 27 May 1997

    Google Scholar 

  • Patent RU 2126049, 10 Feb 1999

    Google Scholar 

  • Patent RU 2238974, 6 Sept 2001

    Google Scholar 

  • Punt PJ, van Biezen N, Conesa A, Albers A, Mangnus J, van den Hondel CA (2002) Filamentous fungi as cell factories for heterologous protein production. Trends Biotechnol 20(5):200–206

    Article  CAS  PubMed  Google Scholar 

  • Serebryanyi VA, Vavilova EA, Chulkin AM, Vinetski YP (2002) Cloning of Penicillium canescens 1,4-b-endoxylanase gene and construction of multicopy strains. Appl Biochem Microbiol (Russ) 38(5):495–501

    Google Scholar 

  • Siebert PD, Chenchik A et al (1995) An improved PCR method for walking in uncloned genomic DNA. Nucleic Acid Res 23(6):1087–1088

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Sinitsyna OA (2002) Properties of recombinant endoglucanase and xylanase from Penicillium. Dissertation, Moscow State University

    Google Scholar 

  • USSR Patent 1065476, 7 Jan 1984

    Google Scholar 

  • USSR Patent 1120700, 4 Nov 1982

    Google Scholar 

  • van Peij NN, Visser J, de Graaff LH (1998a) Isolation and analysis of xlnR, encoding a transcriptional activator co-ordinating xylanolytic expression in Aspergillus niger. Mol Microbiol 27:131–142

    Article  PubMed  Google Scholar 

  • van Peij NN, Gielkens MMC, de Vries RP, Visser J, de Graaff LH (1998b) The transcriptional activator XlnR regulates both xylanolytic and endoglucanase gene expression in Aspergillus niger. Appl Environ Microbiol 64:3615–3619

    PubMed Central  PubMed  Google Scholar 

  • Vavilova EA, Vinetsky YP (2003) Induction of the synthesis of endo-l,4-β-xylanase and β-Galactosidase in the original and recombinant strains of the fungus Penicillium canescens. Appl Biochem Microbiol 39(2):167–172

    Article  CAS  Google Scholar 

  • Vavilova EA, Antonova SV, Barsukov ED, Vinetsky YP (2003) Mechanism of overproduction of secreted enzymes in the mycelial fungus Penicillium canescens. Appl Biochem Microbiol 39(3):284–282

    Article  CAS  Google Scholar 

  • Verdoes JC, Punt PJ, van den Hondel CA (1995) Molecular genetic strain improvement for the overproduction of fungal proteins by filamentous fungi. Appl Microbiol Biotechnol 43(2):195–205

    Article  CAS  Google Scholar 

  • Visser H, Joosten V, Pj P et al (2011) Development of a mature fungal technology and production platform for industrial enzymes based on a Myceliophthora thermophila isolate, previously known as Chrysosporium lucknowense. Ind Biotechnol 7(3):214–223

    Article  CAS  Google Scholar 

  • Volchok AA, Rozhkova AM et al (2012) Application of the new generation enzymatic complexes for treatment of fruit and berries substrates. Wine Winemaking (Russ) 1:20–21

    Google Scholar 

  • Volchok AA, Bushina EV et al (2014) New generation enzymatic complexes for juice industry. Biotechnology (Russia) (in press)

    Google Scholar 

  • Volkov PV (2012) Using of xylA, bgaL and abfA promoters in expression systems for the target protein expression in recombinant Penicillium canescens strains. In: 4th international school of molecular genetic for young scientists, Zvenigorod, 29 Nov–03 Dec 2012

    Google Scholar 

  • Volkov PV, Rozhkova AM, Sinitsyn AP (2010) Creation of the Penicillium canescens gene expression system based on α-L-arabinofuranosidase promoter. In: Abstract of the Moscow international scientific and practical conference “biotechnology: ecology of cities”, Moscow, 15–17 Mar 2010

    Google Scholar 

  • Volkov PV, Rozhkova AM et al (2012a) Production of enzyme preparations on the basis of Penicillum canescens recombinant strains with a high ability for the hydrolysis of plant materials. Appl Biochem Microbiol (Russ) 48(1):66–73

    CAS  Google Scholar 

  • Volkov PV, Sinitsyna OA et al (2012b) Isolation and properties of recombinant inulinases from Aspergillus sp. Biochemistry (Russia) 77(5):492–501

    CAS  Google Scholar 

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Acknowledgments

This study was supported by the Russian Science Foundation (GRANT 14-14-00881).

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Correspondence to Alexandra M. Rozhkova .

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Sinitsyn, A.P., Rozhkova, A.M. (2015). Penicillium canescens Host as the Platform for Development of a New Recombinant Strain Producers of Carbohydrases. In: Kamm, B. (eds) Microorganisms in Biorefineries. Microbiology Monographs, vol 26. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-45209-7_1

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