Purification, characterization and gene cloning of a novel glutamic acid-specific endopeptidase from Staphylococcus aureus ATCC 12600 - PubMed (original) (raw)
Comparative Study
. 1992 May 22;1121(1-2):221-8.
doi: 10.1016/0167-4838(92)90358-k.
Affiliations
- PMID: 1599945
- DOI: 10.1016/0167-4838(92)90358-k
Comparative Study
Purification, characterization and gene cloning of a novel glutamic acid-specific endopeptidase from Staphylococcus aureus ATCC 12600
K Yoshikawa et al. Biochim Biophys Acta. 1992.
Abstract
Twenty strains of Staphylococcus aureus from ATCC type cultures and strains found in clinical studies were cultivated, and their endopeptidase activity specific for glutamic acid was surveyed using benzyloxycarbonyl-Phe-Leu-Glu-p-nitroanilide (Z-Phe-Leu-Glu-pNA) as a substrate. The activity was found in two of the strains, ATCC 12600 and ATCC 25923. A glutamic acid-specific proteinase, which we propose to call SPase, was purified from the culture filtrate of S. aureus strain ATCC 12600 by a series of column chromatographies on DEAE-Sepharose twice and on Sephacryl S-200. A single band was observed on sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) of the purified SPase. The molecular weight of the proteinase was estimated to be 34000 by SDS-PAGE. When synthetic peptides and oxidized insulin B-chain were used as substrates, SPase showed the same substrate specificity as V8 proteinase, EC 3.4.21.9, which specifically cleaves peptide bonds on the C-terminal side of glutamic acid and aspartic acid. Examination with p-nitroanilides of glutamic acid and aspartic acid as substrates, however, revealed that both proteinases are highly specific for a glutamyl bond in comparison with an aspartyl bond. To elucidate the complete primary structure of SPase, its gene was cloned from genomic DNA of S. aureus ATCC 12600, and the nucleotide sequence was determined. Taking the amino acid sequence of SPase from the NH2-terminus to the 27th residue into consideration, the clones encode a mature peptide of 289 amino acids, which follows a prepropeptide of 68 residues. SPase was confirmed to be a novel endopeptidase specific for glutamic acid, being different from V8 proteinase which consists of 268 amino acids.
Similar articles
- Purification, characterization and molecular cloning of an acidic amino acid-specific proteinase from Streptomyces fradiae ATCC 14544.
Kitadokoro K, Nakamura E, Tamaki M, Horii T, Okamoto H, Shin M, Sato T, Fujiwara T, Tsuzuki H, Yoshida N, et al. Kitadokoro K, et al. Biochim Biophys Acta. 1993 May 13;1163(2):149-57. doi: 10.1016/0167-4838(93)90176-r. Biochim Biophys Acta. 1993. PMID: 8490047 - Purification, characterization, cloning, and expression of a glutamic acid-specific protease from Bacillus licheniformis ATCC 14580.
Kakudo S, Kikuchi N, Kitadokoro K, Fujiwara T, Nakamura E, Okamoto H, Shin M, Tamaki M, Teraoka H, Tsuzuki H, et al. Kakudo S, et al. J Biol Chem. 1992 Nov 25;267(33):23782-8. J Biol Chem. 1992. PMID: 1429718 - Genetic and biochemical characterization of glutamyl endopeptidase of Staphylococcus warneri M.
Yokoi K, Kakikawa M, Kimoto H, Watanabe K, Yasukawa H, Yamakawa A, Taketo A, Kodaira KI. Yokoi K, et al. Gene. 2001 Dec 27;281(1-2):115-22. doi: 10.1016/s0378-1119(01)00782-x. Gene. 2001. PMID: 11750133 - Types and families of endopeptidases.
Barrett AJ, Rawlings ND. Barrett AJ, et al. Biochem Soc Trans. 1991 Aug;19(3):707-15. doi: 10.1042/bst0190707. Biochem Soc Trans. 1991. PMID: 1783203 Review. No abstract available. - Proteinases and extracellular matrix remodeling.
Alexander CM, Werb Z. Alexander CM, et al. Curr Opin Cell Biol. 1989 Oct;1(5):974-82. doi: 10.1016/0955-0674(89)90068-9. Curr Opin Cell Biol. 1989. PMID: 2697298 Review. No abstract available.
Cited by
- Hetero- and autoprocessing of the extracellular metalloprotease (Mpr) in Bacillus subtilis.
Park CH, Lee SJ, Lee SG, Lee WS, Byun SM. Park CH, et al. J Bacteriol. 2004 Oct;186(19):6457-64. doi: 10.1128/JB.186.19.6457-6464.2004. J Bacteriol. 2004. PMID: 15375126 Free PMC article. - Purification and characterization of a novel thermoacid-stable fibrinolytic enzyme from Staphylococcus sp. strain AJ isolated from Korean salt-fermented Anchovy-joet.
Choi NS, Song JJ, Chung DM, Kim YJ, Maeng PJ, Kim SH. Choi NS, et al. J Ind Microbiol Biotechnol. 2009 Mar;36(3):417-26. doi: 10.1007/s10295-008-0512-9. Epub 2008 Dec 23. J Ind Microbiol Biotechnol. 2009. PMID: 19104859 - Staphylococcus aureus Secreted Toxins and Extracellular Enzymes.
Tam K, Torres VJ. Tam K, et al. Microbiol Spectr. 2019 Mar;7(2):10.1128/microbiolspec.gpp3-0039-2018. doi: 10.1128/microbiolspec.GPP3-0039-2018. Microbiol Spectr. 2019. PMID: 30873936 Free PMC article. Review. - Bacillus intermedius glutamyl endopeptidase. Molecular cloning and nucleotide sequence of the structural gene.
Rebrikov DV, Akimkina TV, Shevelev AB, Demidyuk IV, Bushueva AM, Kostrov SV, Chestukhina GG, Stepanov VM. Rebrikov DV, et al. J Protein Chem. 1999 Jan;18(1):21-7. doi: 10.1023/a:1020639230985. J Protein Chem. 1999. PMID: 10071925
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous