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PMID: 8597577 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

A study of a series of recombinant fungal laccases and bilirubin oxidase that exhibit significant differences in redox potential, substrate specificity, and stability.

Biochimica et biophysica acta ·Vol. 1292 ·No. 2 ·1996-02-08 ·Pages 303-11

Xu F, Shin W, Brown SH, Wahleithner JA, Sundaram UM, Solomon EI

Abstract

A series of fungal laccases (Polyporus pinsitus, Rhizoctonia solani, Myceliophthora thermophila, Scytalidium thermophilum) and one bilirubin oxidase (Myrothecium verrucaria) have been studied to determine their redox potential, specificity, and stability. Polyporus and Rhizoctonia laccases possess potentials near 0.7-0.8 V (vs. NHE), while other oxidases have potentials near 0.5 V. It is observed that higher redox potential correlates with higher activity. By EPR, no significant change in the geometry of type 1 copper (II) site is observed over this series. At the optimal pH, the two substrates studied, 2,2'-azinobis-(3-ethylbenzthiazoline-6-sulfonic acid) and syringaldazine, show Km values ranging form 10 to 120 and from 1 to 45 microM; and kcat values ranging from 50 to 16 000 and 200 to 3000 per min, respectively. The enzymes are more stable in the neutral-alkaline pH range. The thermal stability is in the order of bilirubin oxidase equivalent to Myceliophthora laccase equivalent to Scytalidium laccase > Polyporus laccase > Rhizoctonia laccase. Based on these results and the sequence alignments made against Zucchini ascorbate oxidase it is speculated that structural differences in the substrate-activation site (a 'blue', type 1 copper center) control the redox potential range as well as substrate specificity, and the cystine content contributes to stability.

MeSH Terms
Electron Spin Resonance Spectroscopy Enzyme Stability Fungi/enzymology Hot Temperature Hydrogen-Ion Concentration Kinetics Laccase Oxidation-Reduction Oxidoreductases/chemistry,isolation & purification,metabolism Oxidoreductases Acting on CH-CH Group Donors Potentiometry Recombinant Proteins/chemistry,isolation & purification,metabolism Species Specificity Spectrophotometry Substrate Specificity Thermodynamics
Chemicals
Recombinant Proteins Oxidoreductases Laccase Oxidoreductases Acting on CH-CH Group Donors bilirubin oxidase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Xu F
Novo Nordisk Biotech, Davis, CA 95616 USA.
Shin W
Brown S H
Wahleithner J A
Sundaram U M
Solomon E I
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1996-02-08
Pages
303-11
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIDDK NIH HHS · DK 31450 · United States
Corrections
ErratumIn
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