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PMID: 831771 Published · ppublish English Journal Article

Properties of L-methionine gamma-lyase from Pseudomonas ovalis.

Biochemistry ·Vol. 16 ·No. 1 ·1977-01-11 ·Pages 100-6

Tanaka H, Esaki N, Soda K

Abstract

The distribution of bacterial L-methionine gamma-lyase (L-methionine methanethiollyase (deaminating) (EC 4.4.1.11) was investigated, and Pseudomonas ovalis (IFO 3738) was found to have the highest activity of enzyme, which was inducibly formed by addition of L-methionine to the medium. L-Methionine gamma-lyase, purified to homogeneity from Ps. ovalis, has a molecular weight of about 173 000 and consists of nonidentical subunits (mol wt: 40 000 and 48 000). The enzyme exhibits absorption maxima at 278 and 420 nm, and a shoulder around 330 nm, which are independent of the pH (6.0 to 10.0), and contains 4 mol of pyridoxal 5'-phosphate per mol of the enzyme. The formyl group of pyridoxal 5'-phosphate is bound in an aldimine linkage to the epsilon-amino group of lysine residues of the protein. The holoenzyme is resolved to the apoenzyme by incubation with hydroxylamine, and reconstituted by addition of pyridoxal 5'-phosphate. The enzyme activity is significantly affected by both carbonyl and sulfhydryl reagents. L-Methionine gamma-lyase catalyzes alpha,gamma- and alpha,beta-elimination reactions of, in addition to L-methionine, several derivatives of L-methionine and L-cysteine, e.g., L-ethionine, DL-methionine sulfone, L-homocysteine, and S-methyl-L-cysteine. The enzyme catalyzes also gamma-replacement reactions of the thiomethyl group of methionine with various alkanethiols (C2-C7), arylthio alcohols (benzenethiol and beta-naphthalenethiol) and the derivatives of ethanethiol (2-mercaptoethanol and cysteamine) to yield the corresponding S-substituted homocysteine. The thiomethyl group of S-methyl-L-cysteine also is replaced by ethanethiol to form S-ethyl-L-cysteine.

MeSH Terms
Carbon-Sulfur Lyases/metabolism Homocysteine/analogs & derivatives Kinetics Lyases/metabolism Macromolecular Substances Magnetic Resonance Spectroscopy Methionine Molecular Weight Oxidation-Reduction Pseudomonas/enzymology Spectrophotometry Spectrophotometry, Ultraviolet Structure-Activity Relationship
Chemicals
Macromolecular Substances Homocysteine Methionine Lyases Carbon-Sulfur Lyases L-methionine gamma-lyase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tanaka H
Esaki N
Soda K
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1977-01-11
Pages
100-6
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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