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PMID: 8955296 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Menaquinone (vitamin K2) biosynthesis: overexpression, purification, and properties of o-succinylbenzoyl-coenzyme A synthetase from Escherichia coli.

Journal of bacteriology ·Vol. 178 ·No. 23 ·1996-12-00 ·Pages 6778-81

Kwon O, Bhattacharyya DK, Meganathan R

Abstract

The coenzyme A (CoA)- and ATP-dependent conversion of o-succinylbenzoic acid [OSB; 4-(2'-carboxyphenyl)-4-oxobutyric acid], to o-succinylbenzoyl-CoA is carried out by the enzyme o-succinylbenzoyl-CoA synthetase. o-Succinylbenzoyl-CoA is a key intermediate in the biosynthesis of menaquinone (vitamin K2) in both gram-negative and gram-positive bacteria. The enzyme has been overexpressed and purified to homogeneity. The purified enzyme was found to have a native molecular mass of 185 kDa as determined by gel filtration column chromatography on Sephacryl S-200. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis established a subunit molecular mass of 49 kDa. Thus, the enzyme is a homotetramer. The enzyme showed a pH optimum of 7.5 to 8.0 and a temperature optimum of 30 to 40 degrees C. The Km values for OSB, ATP, and CoA were 16, 73.5, and 360 microM, respectively. Of the various metal ions tested, Mg2+ was found to be the most effective in stimulating the enzyme activity. Studies with substrate analogs showed that neither benzoic acid nor benzoylpropionic acid (succinylbenzene) is a substrate for the enzyme. Thus, it appears that both the benzoyl carboxyl group and the succinyl side chain are required for activation of the aliphatic carboxyl group.

MeSH Terms
Benzoates/metabolism Cations/pharmacology Escherichia coli/enzymology Hydrogen-Ion Concentration Kinetics Magnesium/pharmacology Molecular Weight Spectrophotometry, Ultraviolet Substrate Specificity Succinate-CoA Ligases/chemistry,genetics,isolation & purification,metabolism Temperature Transformation, Bacterial Vitamin K/biosynthesis
Chemicals
Benzoates Cations Vitamin K Succinate-CoA Ligases O-succinylbenzoate - CoA ligase Magnesium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kwon O
Department of Biological Sciences, Northern Illinois University, DeKalb 60115-2861, USA.
Bhattacharyya D K
Meganathan R
References (13)
13 references, click to expand
  1. Characterization of Escherichia coli men mutants defective in conversion of o-succinylbenzoate to 1,4-dihydroxy-2-naphthoate.
    J Bacteriol. 1982 Dec;152(3):1132-7 PMID: 6754698
  2. A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.
    Proc Natl Acad Sci U S A. 1985 Feb;82(4):1074-8 PMID: 3156376
  3. Use of T7 RNA polymerase to direct expression of cloned genes.
    Methods Enzymol. 1990;185:60-89 PMID: 2199796
  4. o-Succinylbenzoate: coenzyme A ligase, an enzyme involved in menaquinone (vitamin K2) biosynthesis, displays broad specificity.
    Z Naturforsch C. 1991 Jul-Aug;46(7-8):585-90 PMID: 1663748
  5. Menaquinone (vitamin K2) biosynthesis: nucleotide sequence and expression of the menB gene from Escherichia coli.
    J Bacteriol. 1992 Aug;174(15):5057-62 PMID: 1629162
  6. Menaquinone (vitamin K2) biosynthesis: localization and characterization of the menE gene from Escherichia coli.
    Gene. 1996 Feb 2;168(1):43-8 PMID: 8626063
  7. Biosynthesis of vitamin K (menaquinone) in bacteria.
    Microbiol Rev. 1982 Sep;46(3):241-80 PMID: 6127606
  8. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
    Anal Biochem. 1976 May 7;72:248-54 PMID: 942051
  9. Menaquinone biosynthesis: conversion of o-succinylbenzoic acid to 1,4-dihydroxy-2-naphthoic acid and menaquinones by Escherichia coli extracts.
    Biochemistry. 1976 Nov 2;15(22):4792-6 PMID: 791360
  10. Menaquinone (vitamin K2) biosynthesis: conversion of o-succinylbenzoic acid to 1,4-dihydroxy-2-naphthoic acid by Mycobacterium phlei enzymes.
    J Bacteriol. 1979 Oct;140(1):92-8 PMID: 500558
  11. Conversion of o-succinylbenzoate to dihydroxynaphthoate by extracts of Micrococcus luteus.
    Biochemistry. 1980 Feb 19;19(4):785-9 PMID: 7356957
  12. Identification of Bacillus subtilis men mutants which lack O-succinylbenzoyl-coenzyme A synthetase and dihydroxynaphthoate synthase.
    J Bacteriol. 1981 Jan;145(1):328-32 PMID: 6780515
  13. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1996-12-00
Pages
6778-81
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC178575
Subset
IM
Grants
NIGMS NIH HHS · GM50262 · United States
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