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PMID: 1429718 Published · ppublish English Comparative Study Journal Article

Purification, characterization, cloning, and expression of a glutamic acid-specific protease from Bacillus licheniformis ATCC 14580.

The Journal of biological chemistry ·Vol. 267 ·No. 33 ·1992-11-25 ·Pages 23782-8

Kakudo S, Kikuchi N, Kitadokoro K, Fujiwara T, Nakamura E, Okamoto H, Shin M, Tamaki M, Teraoka H, Tsuzuki H

Abstract

A glutamic acid-specific protease has been purified to homogeneity from Bacillus licheniformis ATCC 14580 utilizing Phe-Leu-D-Glu-OMe-Sepharose affinity chromatography and crystallized. The molecular weight of the protease was estimated to be approximately 25,000 by SDS-polyacrylamide gel electrophoresis. This protease, which we propose to call BLase (glutamic acid-specific protease from B. licheniformis ATCC 14580), was characterized enzymatically. Using human parathyroid hormone (13-34) and p-nitroanilides of peptidyl glutamic acid and aspartic acid, we found a marked difference between BLase and V8 protease, EC 3.4.21.9, although both proteases showed higher reactivity for glutamyl bonds than for aspartyl bonds. Diisopropyl fluorophosphate and benzyloxycarbonyl Leu-Glu chloromethyl ketone completely inhibited BLase, whereas EDTA reversibly inactivated the enzyme. The findings clearly indicate that BLase can be classified as a serine protease. To elucidate the complete primary structure and precursor of BLase, its gene was cloned from the genomic DNA of B. licheniformis ATCC 14580, and the nucleotide sequence was determined. Taking the amino-terminal amino acid sequence of the purified BLase into consideration, the clones encode a mature peptide of 222 amino acids, which follows a prepropeptide of 94 residues. The recombinant BLase was expressed in Bacillus subtilis and purified to homogeneity. Its key physical and chemical characteristics were the same as those of the wild-type enzyme. BLase was confirmed to be a protease specific for glutamic acid, and the primary structure deduced from the cDNA sequence was found to be identical with that of a glutamic acid-specific endopeptidase isolated from Alcalase (Svendsen, I., and Breddam, K. (1992) Eur. J. Biochem. 204, 165-171), being different from V8 protease and the Glu-specific protease of Streptomyces griseus which consist of 268 and 188 amino acids, respectively.

MeSH Terms
Amino Acid Sequence Animals Bacillus/enzymology,genetics Bacterial Proteins Base Sequence Cattle Chromatography, Affinity Chromatography, Gel Chromatography, Ion Exchange Chymotrypsin/genetics Cloning, Molecular Electrophoresis, Polyacrylamide Gel Kinetics Molecular Sequence Data Oligodeoxyribonucleotides Oligopeptides/metabolism Polymerase Chain Reaction/methods Recombinant Proteins/isolation & purification,metabolism Sequence Homology, Amino Acid Serine Endopeptidases/genetics,isolation & purification,metabolism Substrate Specificity Trypsin/genetics
Chemicals
Bacterial Proteins Oligodeoxyribonucleotides Oligopeptides Recombinant Proteins Serine Endopeptidases Chymotrypsin blaSE protein, Bacillus licheniformis Trypsin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Kakudo S
Shionogi Research Laboratories, Shionogi and Co., Ltd., Osaka, Japan.
Kikuchi N
Kitadokoro K
Fujiwara T
Nakamura E
Okamoto H
Shin M
Tamaki M
Teraoka H
Tsuzuki H
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-11-25
Pages
23782-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
D10060, D12748, D12749, D12750, D12751, D12752, D12753, L01089, L01090, M95819
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