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非核糖体肽合成酶HMWP2在鼠疫耶尔森菌的铁螯合毒力因子耶尔森菌素的生物合成过程中形成一个噻唑啉环。

The nonribosomal peptide synthetase HMWP2 forms a thiazoline ring during biogenesis of yersiniabactin, an iron-chelating virulence factor of Yersinia pestis.

作者信息

Gehring A M, Mori I, Perry R D, Walsh C T

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Biochemistry. 1998 Aug 18;37(33):11637-50. doi: 10.1021/bi9812571.

Abstract

Pathogenic Yersinia species have been shown to synthesize a siderophore molecule, yersiniabactin, as a virulence factor during iron starvation. Here we provide the first biochemical evidence for the role of the Yersinia pestis high molecular weight protein 2 (HMWP2), a nonribosomal peptide synthetase homologue, and YbtE in the initiation of yersiniabactin biosynthesis. YbtE catalyzes the adenylation of salicylate and the transfer of this activated salicyl group to the N-terminal aryl carrier protein domain (ArCP; residues 1-100) of HMWP2. A fragment of HMWP2, residues 1-1491, can adenylate cysteine and with the resulting cysteinyl-AMP autoaminoacylate the peptidyl carrier protein domain (PCP1; residues 1383-1491) either in cis or in trans. Catalytic release of hydroxyphenylthiazoline carboxylic acid (HPT-COOH) and/or N-(hydroxyphenylthiazolinylcarbonyl)cysteine (HPT-cys) is observed upon incubation of YbtE, HMWP2 1-1491, L-cysteine, salicylate, and ATP. These products presumably arise from nucleophilic attack by water or cysteine of a stoichiometric hydroxyphenylthiazolinylcarbonyl-S-PCP1-HMWP2 intermediate. Detection of the heterocyclization capacity of HMWP2 1-1491 implies salicyl-transferring and thiazoline-forming activity for the HMWP2 condensation domain (residues 101-544) and is the first demonstration of such heterocyclization ability in a nonribosomal peptide synthetase enzyme.

摘要

致病性耶尔森菌属物种已被证明在缺铁期间会合成一种铁载体分子——耶尔森菌素,作为一种毒力因子。在此,我们首次提供了生化证据,证明鼠疫耶尔森菌高分子量蛋白2(HMWP2,一种非核糖体肽合成酶同源物)和YbtE在耶尔森菌素生物合成起始过程中的作用。YbtE催化水杨酸的腺苷化,并将这种活化的水杨酰基转移到HMWP2的N端芳基载体蛋白结构域(ArCP;第1 - 100位氨基酸残基)。HMWP2的一个片段,第1 - 1491位氨基酸残基,能够使半胱氨酸腺苷化,并使生成的半胱氨酰 - AMP在顺式或反式情况下对肽基载体蛋白结构域(PCP1;第1383 - 1491位氨基酸残基)进行自身氨酰化。在将YbtE、HMWP2 1 - 1491、L - 半胱氨酸、水杨酸和ATP一起孵育时,可观察到羟基苯基噻唑啉羧酸(HPT - COOH)和/或N -(羟基苯基噻唑啉基羰基)半胱氨酸(HPT - cys)的催化释放。这些产物可能是由化学计量的羟基苯基噻唑啉基羰基 - S - PCP1 - HMWP2中间体受到水或半胱氨酸的亲核攻击而产生的。对HMWP2 1 - 1491杂环化能力的检测表明,HMWP2缩合结构域(第101 - 544位氨基酸残基)具有水杨酰转移和噻唑啉形成活性,这是在非核糖体肽合成酶中首次证明这种杂环化能力。

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