PHYSIOLOGY AND MOLECULAR-BIOLOGY OF THE LIGNIN PEROXIDASES OF PHANEROCHAETE-CHRYSOSPORIUM

Citation
Ca. Reddy et Tm. Dsouza, PHYSIOLOGY AND MOLECULAR-BIOLOGY OF THE LIGNIN PEROXIDASES OF PHANEROCHAETE-CHRYSOSPORIUM, FEMS microbiology reviews, 13(2-3), 1994, pp. 137-152
Citations number
95
Categorie Soggetti
Microbiology
Journal title
ISSN journal
01686445
Volume
13
Issue
2-3
Year of publication
1994
Pages
137 - 152
Database
ISI
SICI code
0168-6445(1994)13:2-3<137:PAMOTL>2.0.ZU;2-B
Abstract
The white-rot basidiomycete Phanerochaete chrysosporium produces ligni n peroxidases (LiPs), a family of extracellular glycosylated heme prot eins, as major components of its lignin-degrading system. Upto 15 LiP isozymes, ranging in M(r) values from 38000 to 43000, are produced dep ending on culture conditions and strains employed. Manganese-dependent peroxidases (MnPs) are a second family of extracellular heme proteins produced by P. chrysosporium that are also believed to be important i n lignin degradation by this organism. LiP and MnP production is seen during secondary metabolism and is completely suppressed under conditi ons of excess nitrogen and carbon. Excess Mn(II) in the medium, on the other hand, suppresses LiP production but enhances MnP production. Ni trogen regulation of LiP and MnP production is independent of carbon a nd Mn(II) regulation. LiP activity is also affected by idiophasic extr acellular proteases. Intracellular cAMP levels appear to be important in regulating the production of LiPs and MnPs, although LiP production is affected,more than MnP production. Studies on the sequencing and c haracterization of lip cDNAs and genes of P. chrysosporium have shown that the major LiP isozymes are each encoded by a separate gene. Each lip gene encodes a mature protein that is 343-344 amino acids long, co ntains 1 putative N-glycosylation site, a number of putative O-glycosy lation sites, and is preceded by a 27-28-amino acid leader peptide end ing in a Lys-Arg cleavage site. The coding region of each lip gene is interrupted by 8-9 introns (50-63 bp), and the positions of the last t wo introns appear to be highly conserved. There are substantial differ ences in the temporal transcription patterns of the major lip genes. T he sequence data suggest the presence of three lip gene subfamilies. T he genomic DNA of P. chrysosporium strain BKMF-1767 was resolved into 10 chromosomes (genome size of 29 Mb), and that of strain ME-446 into 11 chromosomes (genome size of 32 Mb). The lip genes have been localiz ed to five chromosomes in BKMF-1767 and to four chromosomes in ME-446. DNA transformation studies have reported both integrative and non-int egrative transformation in P. chrysosporium.