综述或非传感器论文 2011 非传感器论文

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

Microbiology (Reading, England) Wahjudi M, Papaioannou E, Hendrawati O, van Assen AHG, van Merkerk R, Cool RH, Poelarends GJ, Quax WJ
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组成图示

PA0305 of Pseudomonas aeruginosa is a... 传感器构成示意图

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传感器类型

综述或非传感器论文

检测对象

酰基高丝氨酸内酯(AHLs,含 C4-HSL、C6-HSL、3-oxo-C6-HSL、C7-HSL、C8-HSL、3-oxo-C8-HSL、C10-HSL、3-oxo-C10-HSL、C12-HSL、3-oxo-C12-HSL、C14-HSL、3-oxo-C14-HSL);样品基质:PBS 缓冲液、大肠杆菌无细胞提取物、铜绿假单胞菌 LB 培养上清

检测原理

该检测采用大肠杆菌全细胞生物发光生物传感器。待测 AHL 进入 E. coli JM109 后,与 pSB401、pSB536 或 pSB1075 质粒编码的 AHL 响应受体结合,形成 AHL-受体复合物,激活 AHL 响应启动子,驱动 lux 报告基因表达。荧光素酶催化底物氧化产生生物发光,发光强度以 RLU 读出,通常随 AHL 浓度升高而增强。若样品中存在 PA0305 等 AHL 酰基酶,AHL 酰胺键被水解为高丝氨酸内酯和酰基酸,剩余 AHL 减少,生物发光相应降低。该体系通过受体识别、启动子激活和荧光素酶催化实现信号放大。

检测灵敏度

原文未报告 LOD、线性范围、灵敏度斜率或相关系数。

效应效果

PA0305 可降解 C6–C14 碳链 AHLs,对 C4-HSL 无活性;10 µg/ml C8-HSL 时发光降低 93 倍,0.01 µg/ml 3-oxo-C12-HSL 时降低 64 倍。其对 3-oxo-C12-HSL 的表观 Kcat/Km 为 7.8×10^4 M^-1 s^-1,比 C8-HSL 高 56 倍。Δpa0305 菌株 50 h 后 3-oxo-C12-HSL 积累升高,三重缺失株较双重缺失株约增加 250%。过表达 pa0305 降低弹性蛋白酶和绿脓菌素,不影响 C4-HSL。线虫模型中,缺失株第 7 天存活率约 41%,野生型和过表达株约 57%,P<0.05。

传感器的构成

  • 传感基质:96孔微孔板(Lumitrac600)与 PBS 缓冲液,承载样品、酶反应及生物传感器细胞
  • 宿主细胞:E. coli JM109,作为全细胞 AHL 生物传感器,表达报告系统并产生生物发光
  • 报告质粒:pSB401、pSB536 或 pSB1075,分别响应 C6–C8-HSL、C4-HSL 或 C10–C14-HSL 及其 3-oxo 形式
  • 识别元件:pSB 质粒编码的 AHL 响应受体,结合 AHL 并启动 AHL 响应启动子
  • 信号元件:pSB 质粒携带的 lux 报告基因,表达荧光素酶并产生生物发光
  • 读出装置:FLUOstar Omega 微孔板读数仪,检测相对发光单位(RLU)

中文摘要

铜绿假单胞菌 PAO1 基因组至少含有 pvdQ 和 quiP 两个编码酰基高丝氨酸内酯(AHL)酰基酶的基因;pa1893 和 pa0305 曾被预测编码青霉素酰基酶但功能未明。前期转座子突变体研究提示 pa0305 与 AHL 生长表型无关。由于 pa0305 与 Pseudomonas syringae 的 AHL 酰基酶 HacB 具有 67% 序列相似性,作者克隆并过量表达 pa0305,纯化 PA0305 并进行功能表征。纯化蛋白经翻译后加工形成 α 和 β 亚基,催化丝氨酸位于 β 亚基 N 端,表明其属于 N 端亲核水解酶超家族。利用大肠杆菌 lux 生物传感器检测,PA0305 可降解酰基链长度为 6–14 个碳的 AHLs。以 C8-HSL 和 3-oxo-C12-HSL 为底物的动力学研究显示,其表观 Kcat/Km 分别为 0.14×10^4 M^-1 s^-1 和 7.8×10^4 M^-1 s^-1。在铜绿假单胞菌中过表达 pa0305 可显著降低 3-oxo-C12-HSL 积累和毒力因子表达;Δpa0305 突变体对秀丽隐杆线虫的致死能力略强于野生型和过表达株。结论:pa0305 编码一种高效长链 AHL 酰基酶,建议命名为 HacB。

英文摘要

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.