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Cloning and expression in Bacillus subtilis of the npr gene from Bacillus thermoproteolyticus Rokko coding for the thermostable metalloprotease thermolysin.

作者信息

O'Donohue M J, Roques B P, Beaumont A

机构信息

Laboratoire de Pharmacochimie Moléculaire et Structurale, CNRS URA D1500, INSERM U266, Faculté de Pharmacie, Université Paris V, France.

出版信息

Biochem J. 1994 Jun 1;300 ( Pt 2)(Pt 2):599-603. doi: 10.1042/bj3000599.

DOI:10.1042/bj3000599
PMID:8002967
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1138203/
Abstract

We report the isolation, cloning and expression, in Bacillus subtilis, of the gene coding for thermolysin, a thermostable metalloprotease which is produced by Bacillus thermoproteolyticus Rokko. The nucleotide sequence has revealed that, like neutral proteases produced by other members of the Bacillus species, thermolysin is probably produced as a preproenzyme carrying a typical N-terminal membrane signal sequence. Further, the thermolysin gene shares a strong homology with two other previously cloned genes from two different strains of Bacillus stearothermophilus. The sequence of the mature secreted protease, inferred from the DNA sequence, is, with two exceptions, identical with the previously published protein sequence of thermolysin [Titani, Hermodson, Ericsson, Walsh and Neurath (1972) Nature (London) 238, 35-37]. The exceptions are Asn37 and Gln119, originally reported to be Asp and Glu respectively. The biochemical characterization of the secreted recombinant protein shows that it is indistinguishable from the wild-type thermolysin.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8439/1138203/07aa915f5c50/biochemj00086-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8439/1138203/c8c0880b5910/biochemj00086-0312-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8439/1138203/07aa915f5c50/biochemj00086-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8439/1138203/c8c0880b5910/biochemj00086-0312-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8439/1138203/07aa915f5c50/biochemj00086-0313-a.jpg

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Biotechniques. 1993 Apr;14(4):532-4, 536.
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Neutral endopeptidase 24.11: structure, inhibition, and experimental and clinical pharmacology.中性内肽酶24.11:结构、抑制作用以及实验与临床药理学
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Protein secretion in Bacillus species.芽孢杆菌属中的蛋白质分泌
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Refined 1.8 A X-ray crystal structure of astacin, a zinc-endopeptidase from the crayfish Astacus astacus L. Structure determination, refinement, molecular structure and comparison with thermolysin.精制的1.8埃小龙虾(Astacus astacus L.)锌内肽酶虾红素的X射线晶体结构。结构测定、精制、分子结构及与嗜热菌蛋白酶的比较。
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Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction.抑制常数(K1)与导致酶促反应50%抑制率(I50)的抑制剂浓度之间的关系。
Biochem Pharmacol. 1973 Dec 1;22(23):3099-108. doi: 10.1016/0006-2952(73)90196-2.
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Cloning and nucleotide sequence of the highly thermostable neutral protease gene from Bacillus stearothermophilus.嗜热脂肪芽孢杆菌高耐热中性蛋白酶基因的克隆与核苷酸序列分析
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