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Production and characterization of cellobiohydrolase from a novel strain of Penicillium purpurogenum KJS506

Authors
 Kyoung-Mi Lee  ;  Ah-Reum Joo  ;  Marimuthu Jeya  ;  Kyoung-Min Lee  ;  Hee-Jung Moon  ;  Jung-Kul Lee 
Citation
 APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, Vol.163(1) : 25-39, 2011 
Journal Title
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
ISSN
 0273-2289 
Issue Date
2011
MeSH
Amino Acid Sequence ; Cellulose 1,4-beta-Cellobiosidase/chemistry* ; Cellulose 1,4-beta-Cellobiosidase/genetics ; Cellulose 1,4-beta-Cellobiosidase/isolation & purification ; Cellulose 1,4-beta-Cellobiosidase/metabolism* ; Enzyme Stability ; Fungal Proteins/chemistry* ; Fungal Proteins/genetics ; Fungal Proteins/isolation & purification ; Fungal Proteins/metabolism* ; Molecular Sequence Data ; Penicillium/classification ; Penicillium/enzymology* ; Penicillium/genetics ; Penicillium/isolation & purification* ; Phylogeny ; Sequence Alignment ; Soil Microbiology
Abstract
A high cellobiohydrolase (CBH)-producing strain was isolated and identified as Penicillium purpurogenum KJS506 according to the morphology and comparison of internal transcribed spacer rDNA gene sequence. When rice straw and corn steep powder were used as carbon and nitrogen sources, respectively, a maximum CBH activity of 2.6 U mg-protein(-1), one of the highest among CBH-producing microorganisms, was obtained. The optimum temperature and pH for CBH production were 30 °C and 4.0, respectively. The increased production of CBH in P. purpurogenum culture at 30 °C was confirmed by two-dimensional electrophoresis followed by MS/MS sequencing of the partial peptide. The internal amino acid sequences of P. purpurogenum CBH showed a significant homology with hydrolases from glycoside hydrolase family 7. The extracellular CBH was purified to homogeneity by sequential chromatography of P. purpurogenum culture supernatants on a DEAE-sepharose column, a gel filtration column, and then on a Mono Q column with fast-protein liquid chromatography. The purified CBH was a monomeric protein with a molecular weight of 60 kDa and showed broad substrate specificity with maximum activity towards p-nitrophenyl β-D: -cellobiopyranoside. P. purpurogenum CBH showed t (1/2) value of 4 h at 60 °C and V (max) value of 11.9 μmol min(-1) mg-protein(-1) for p-nitrophenyl-D: -cellobiopyranoside. Although CBHs have been reported, the high specific activity distinguishes P. purpurogenum CBH.
Full Text
https://link.springer.com/article/10.1007/s12010-010-9013-1
DOI
10.1007/s12010-010-9013-1
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Lee, Kyoung Mi(이경미) ORCID logo https://orcid.org/0000-0002-9038-8162
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/158237
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