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PMID: 14240970 Published · ppublish English Journal Article

USE OF S-METHYLCYSTINE AND CYSTATHIONINE BY METHIONINELESS NEUROSPORA MUTANTS.

Journal of bacteriology ·Vol. 88 ·1964-12-00 ·Pages 1798-804

WIEBERS JL, GARNER HR

Abstract

Wiebers, Joyce L. (Purdue University, West Lafayette, Ind.), and Harold R. Garner. Use of S-methylcysteine and cystathionine by methionineless Neurospora mutants. J. Bacteriol. 88:1798-1804. 1964.-Radioactive methionine was found in hydrolysates of various strains of Neurospora crassa when either S-methylcysteine (SMC)-C(14)H(3) or SMC-S(35) is the sole addition to minimal medium. Isotope product-precursor specific activity ratios are very similar for the two sources of label. Wild-type and methionineless mutants use sulfur from SMC in the biosynthesis of methionine, but not of cysteine, when grown in regular medium. With a medium nearly free from sulfate, SMC served as a source of sulfur for both cysteine and methionine. Suppressed methionineless mutants incorporated sulfur from SMC into cellular cysteine even in the presence of normal amounts of sulfate. SMC as a possible metabolic precursor of methionine was compared to cystathionine in an experiment with wild-type Neurospora. The four sources of label used were: SMC-C(14)H(3), SMC-S(35), cystathionine-U-C(14), and cystathionine-S(35). In each flask, the organism was offered one of the labeled compounds plus an equivalent amount of the other compound without label. The amount of each compound was sufficient for either to supply its contribution to all of the cellular methionine, if it were successful in competing with endogenous sources. To avoid adaptive breakdown of substrates, the compounds were added continuously at a rate consistent with the amount of growth present. The ratio of specific activity of cellular methionine to precursor was determined for each labeled compound. The results show that SMC sulfur and methyl carbon are used equally well. Cystathionine carbon and sulfur appear to be equally utilized also. A preference for cystathionine is indicated.

Keywords
AMINO ACID METABOLISM CARBON ISOTOPES CYSTEINE EXPERIMENTAL LAB STUDY GENETICS METHIONINE MUTAGENS MUTATION NEUROSPORA SULFUR ISOTOPES
MeSH Terms
Amino Acids/metabolism Carbon Isotopes Cystathionine Cysteine Genetics Methionine Mutagens Mutation Neurospora Research Sulfur Sulfur Isotopes
Chemicals
Amino Acids Carbon Isotopes Mutagens Sulfur Isotopes Cystathionine Sulfur S-methylcysteine Methionine Cysteine mecysteine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
WIEBERS J L
GARNER H R
References (5)
5 references, click to expand
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    J Biol Chem. 1954 Dec;211(2):907-13 PMID: 13221596
  2. S-methyl-L-cysteine as a naturally occurring metabolite in Neurospora crassa.
    Arch Biochem Biophys. 1956 Dec;65(2):574-6 PMID: 13395513
  3. Microbial transsulfuration: the mechanism of an enzymatic disulfide elimination reaction.
    J Biol Chem. 1962 Mar;237:768-77 PMID: 13893449
  4. Further evidence on the identity of cystathionase and cysteine desulfhydrase.
    Arch Biochem Biophys. 1963 May;101:363-4 PMID: 13936015
  5. Methionine synthesis in Neurospora crassa.
    Biochem J. 1961 Nov;81:317-9 PMID: 13883171
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1964-12-00
Pages
1798-804
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC277486
Subset
OM
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