AMINO-ACID-SEQUENCE OF COPRINUS-MACRORHIZUS PEROXIDASE AND CDNA SEQUENCE ENCODING COPRINUS-CINEREUS PEROXIDASE - A NEW FAMILY OF FUNGAL PEROXIDASES

被引:58
作者
BAUNSGAARD, L
DALBOGE, H
HOUEN, G
RASMUSSEN, EM
WELINDER, KG
机构
[1] UNIV COPENHAGEN,INST BIOCHEM GENET,OSTER FARIMAGSGADE 2A,DK-1353 COPENHAGEN,DENMARK
[2] NOVO NORDISK AS,BAGSVAERD,DENMARK
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1993年 / 213卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1993.tb17800.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sequence analysis and cDNA cloning of Coprinus peroxidase (CIP) were undertaken to expand the understanding of the relationships of structure, function and molecular genetics of the secretory heme peroxidases from fungi and plants. Amino acid sequencing of Coprinus macrorhizus peroxidase, and cDNA sequencing of Coprinus cinereus peroxidase showed that the mature proteins are identical in amino acid sequence, 343 residues in size and preceded by a 20-residue signal peptide. Their likely identity to peroxidase from Arthromyces ramosus is discussed. CIP has an 8-residue, glycine-rich N-terminal extension blocked with a pyroglutamate residue which is absent in other fungal peroxidases. The presence of pyroglutamate, formed by cyclization of glutamine, and the finding of a minor fraction of a variant form lacking the N-terminal residue, indicate that signal peptidase cleavage is followed by further enzymic processing. CIP is 40 - 45 % identical in amino-acid sequence to 11 lignin peroxidases from four fungal species, and 42 - 43 % identical to the two known Mn-peroxidases. Like these white-rot fungal peroxidases, CIP has an additional segment of approximately 40 residues at the C-terminus which is absent in plant peroxidases. Although CIP is much more similar to horseradish peroxidase (HRP C) in substrate specificity, specific activity and pH optimum than to white-rot fungal peroxidases, the sequences of CIP and HRP C showed only 18% identity. Hence, CIP qualifies as the first member of a new family of fungal peroxidases. The nine invariant residues present in all plant, fungal and bacterial heme peroxidases are also found in CIP. The present data support the hypothesis that only one chromosomal CIP gene exists. In contrast, a large number of secretory plant and fungal peroxidases are expressed from several peroxidase gene clusters. Analyses of three batches of CIP protein and of 49 CIP clones revealed the existence of only two highly similar alleles indicating less peroxidase polymorphism in C cinereus strains than observed in plants and white-rot fungi.
引用
收藏
页码:605 / 611
页数:7
相关论文
共 46 条
[1]   LUMINOL CHEMILUMINESCENCE REACTION CATALYZED BY A MICROBIAL PEROXIDASE [J].
AKIMOTO, K ;
SHINMEN, Y ;
SUMIDA, M ;
ASAMI, S ;
AMACHI, T ;
YOSHIZUMI, H ;
SAEKI, Y ;
SHIMIZU, S ;
YAMADA, H .
ANALYTICAL BIOCHEMISTRY, 1990, 189 (02) :182-185
[2]   SPECTRAL AND KINETIC-PROPERTIES OF OXIDIZED INTERMEDIATES OF COPRINUS-CINEREUS PEROXIDASE [J].
ANDERSEN, MB ;
HSUANYU, Y ;
WELINDER, KG ;
SCHNEIDER, P ;
DUNFORD, HB .
ACTA CHEMICA SCANDINAVICA, 1991, 45 (10) :1080-1086
[3]   KINETICS AND EQUILIBRIA OF CYANIDE BINDING TO COPRINUS-CINEREUS PEROXIDASE [J].
ANDERSEN, MB ;
HSUANYU, YC ;
WELINDER, KG ;
SCHNEIDER, P ;
DUNFORD, HB .
ACTA CHEMICA SCANDINAVICA, 1991, 45 (02) :206-211
[4]  
ANDERSEN MB, 1991, BIOCH MOL PHYSL ASPE, P169
[5]   CHARACTERIZATION OF 2 LIGNIN PEROXIDASE CLONES FROM PHANEROCHAETE-CHRYSOSPORIUM [J].
ANDRAWIS, A ;
PEASE, EA ;
KUAN, IC ;
HOLZBAUR, E ;
TIEN, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 162 (02) :673-680
[6]  
[Anonymous], 1992, CURR OPIN STRUC BIOL, DOI [DOI 10.1016/0959-440X(92)90230-5, 10.1016/0959-440x(92)90230-5]
[7]   ASCORBATE PEROXIDASE - A HYDROGEN PEROXIDE-SCAVENGING ENZYME IN PLANTS [J].
ASADA, K .
PHYSIOLOGIA PLANTARUM, 1992, 85 (02) :235-241
[8]   ENVIRONMENTAL ASPECTS OF MORTIERELLA-WOLFII INFECTION IN CATTLE [J].
AUSTWICK, PKC .
NEW ZEALAND JOURNAL OF AGRICULTURAL RESEARCH, 1976, 19 (01) :25-33
[10]   SEQUENCES IMPORTANT FOR GENE-EXPRESSION IN FILAMENTOUS FUNGI [J].
BALLANCE, DJ .
YEAST, 1986, 2 (04) :229-236