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铜绿假单胞菌 PA0305 是一种群体感应淬灭酰基高丝氨酸内酯酶,属于 Ntn 水解酶超家族。

PA0305 of Pseudomonas aeruginosa is a quorum quenching acylhomoserine lactone acylase belonging to the Ntn hydrolase superfamily.

机构信息

Faculty of Technobiology, University of Surabaya, Indonesia.

Department of Pharmaceutical Biology, University of Groningen, 9713AV Groningen, The Netherlands.

出版信息

Microbiology (Reading). 2011 Jul;157(Pt 7):2042-2055. doi: 10.1099/mic.0.043935-0. Epub 2011 Mar 3.

Abstract

The Pseudomonas aeruginosa PAO1 genome has at least two genes, pvdQ and quiP, encoding acylhomoserine lactone (AHL) acylases. Two additional genes, pa1893 and pa0305, have been predicted to encode penicillin acylase proteins, but have not been characterized. Initial studies on a pa0305 transposon insertion mutant suggested that the gene is not related to the AHL growth phenotype of P. aeruginosa. The close similarity (67 %) of pa0305 to HacB, an AHL acylase of Pseudomonas syringae, prompted us to investigate whether the PA0305 protein might also function as an AHL acylase. The pa0305 gene has been cloned and the protein (PA0305) has been overproduced, purified and subjected to functional characterization. Analysis of the purified protein showed that, like β-lactam acylases, PA0305 undergoes post-translational processing resulting in α- and β-subunits, with the catalytic serine as the first amino acid of the β-subunit, strongly suggesting that PA0305 is a member of the N-terminal nucleophile hydrolase superfamily. Using a biosensor assay, PA0305his was shown to degrade AHLs with acyl side chains ranging in length from 6 to 14 carbons. Kinetics studies using N-octanoyl-L-homoserine lactone (C(8)-HSL) and N-(3-oxo-dodecanoyl)-L-homoserine lactone (3-oxo-C(12)-HSL) as substrates showed that the enzyme has a robust activity towards these two AHLs, with apparent K(cat)/K(m) values of 0.14 × 10(4) M(-1) s(-1) towards C(8)-HSL and 7.8 × 10(4) M(-1 )s(-1) towards 3-oxo-C(12)-HSL. Overexpression of the pa0305 gene in P. aeruginosa showed significant reductions in both accumulation of 3-oxo-C(12)-HSL and expression of virulence factors. A mutant P. aeruginosa strain with a deleted pa0305 gene showed a slightly increased capacity to kill Caenorhabditis elegans compared with the P. aeruginosa PAO1 wild-type strain and the PAO1 strain carrying a plasmid overexpressing pa0305. The harmful effects of the Δpa0305 strain on the animals were most visible at 5 days post-exposure and the mortality rate of the animals fed on the Δpa0305 strain was faster than for the animals fed on either the wild-type strain or the strain overexpressing pa0305. In conclusion, the pa0305 gene encodes an efficient acylase with activity towards long-chain homoserine lactones, including 3-oxo-C(12)-HSL, the natural quorum sensing signal molecule in P. aeruginosa, and we propose to name this acylase HacB.

摘要

铜绿假单胞菌 PAO1 基因组至少有两个基因,pvdQ 和 quiP,编码酰基高丝氨酸内酯(AHL)酰基酶。另外两个基因,pa1893 和 pa0305,被预测编码青霉素酰化酶蛋白,但尚未进行特征描述。对 pa0305 转座子插入突变体的初步研究表明,该基因与铜绿假单胞菌的 AHL 生长表型无关。pa0305 与 Pseudomonas syringae 的 AHL 酰基酶 HacB 的高度相似性(67%)促使我们研究 PA0305 蛋白是否也能作为 AHL 酰基酶发挥作用。已经克隆了 pa0305 基因,并对其编码的蛋白质(PA0305)进行了过表达、纯化和功能表征。对纯化蛋白的分析表明,与β-内酰胺酰基酶一样,PA0305 经历了翻译后加工,产生α-和β-亚基,催化丝氨酸是β-亚基的第一个氨基酸,这强烈表明 PA0305 是 N-末端亲核水解酶超家族的成员。使用生物传感器测定法,PA0305his 被证明可以降解具有 6 至 14 个碳原子长的酰基侧链的 AHLs。使用 N-辛酰基-L-高丝氨酸内酯(C(8)-HSL)和 N-(3-氧代-十二烷酰基)-L-高丝氨酸内酯(3-氧代-C(12)-HSL)作为底物的动力学研究表明,该酶对这两种 AHL 具有很强的活性,对 C(8)-HSL 的表观 Kcat/Km 值为 0.14×10(4)M(-1)s(-1),对 3-氧代-C(12)-HSL 的表观 Kcat/Km 值为 7.8×10(4)M(-1)s(-1)。在铜绿假单胞菌中过表达 pa0305 基因可显著降低 3-氧代-C(12)-HSL 的积累和毒力因子的表达。与铜绿假单胞菌 PAO1 野生型菌株和过表达 pa0305 的 PAO1 菌株相比,缺失 pa0305 基因的铜绿假单胞菌突变株对秀丽隐杆线虫的杀伤能力略有增强。与喂食野生型菌株或过表达 pa0305 的菌株的动物相比,喂食 Δpa0305 菌株的动物在接触后 5 天的毒性作用最为明显,且动物的死亡率更快。综上所述,pa0305 基因编码一种高效的酰基酶,对包括 3-氧代-C(12)-HSL 在内的长链高丝氨酸内酯具有活性,3-氧代-C(12)-HSL 是铜绿假单胞菌中天然的群体感应信号分子,我们建议将这种酰基酶命名为 HacB。

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