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GacS-Dependent Regulation of Polyhydroxyalkanoate Synthesis in Pseudomonas putida CA-3

机译:恶臭假单胞菌CA-3中多羟基链烷酸酯合成的GacS依赖性调控。

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To date, limited reports are available on the regulatory systems exerting control over bacterial synthesis of the biodegradable polyester group known as polyhydroxyalkanoates (PHAs). In this study, we performed random mini-Tn5 mutagenesis of the Pseudomonas putida CA-3 genome and screened transconjugants on nitrogen-limited medium for reduced PHA accumulation phenotypes. Disruption of a GacS sensor kinase in one such mutant was found to eliminate medium-chain-length PHA production in Pseudomonas putida CA-3. Recombinant expression of wild-type gacS from a pBBRgacS vector fully restored PHA accumulation capacity in the mutant strain. PCR-based screening of the P. putida CA-3 genome identified gene homologues of the GacS/GacA-rsm small RNA (sRNA) regulatory cascade with 96% similarity to published P. putida genomes. However, reverse transcription-PCR (RT-PCR) analyses revealed active transcription of the rsmY and rsmZ sRNAs in gacS-disrupted P. putida CA-3, which is atypical of the commonly reported Gac/Rsm regulatory cascade. Quantitative real-time RT-PCR analyses of the phaC1 synthase responsible for polymer formation in P. putida CA-3 indicated no statistically significant difference in transcript levels between the wild-type and gacS-disrupted strains. Subsequently, SDS-PAGE protein analyses of these strains identified posttranscriptional control of phaC1 synthase as a key aspect in the regulation of PHA synthesis by P. putida CA-3.
机译:迄今为止,关于调节系统的报道有限,该调节系统控制了被称为聚羟基链烷酸酯(PHA)的可生物降解聚酯基团的细菌合成。在这项研究中,我们进行了恶臭假单胞菌CA-3基因组的随机mini-Tn5诱变,并在氮限制培养基上筛选了转导结合体,以减少PHA积累表型。发现在一个这样的突变体中GacS传感器激酶的破坏消除了恶臭假单胞菌CA-3中中等链长的PHA产生。来自pBBRgacS载体的野生型gacS的重组表达完全恢复了突变菌株中PHA的积累能力。基于PCR的恶臭假单胞菌CA-3基因组筛选确定了GacS / GacA-rsm小RNA(sRNA)调控级联的基因同源物,与已发表的恶臭假单胞菌基因组有96%的相似性。然而,逆转录PCR(RT-PCR)分析显示,在破坏了gacS的恶臭假单胞菌CA-3中rsmY和rsmZ sRNA的活跃转录,这与通常报道的Gac / Rsm调控级联反应是不典型的。负责恶臭假单胞菌CA-3中聚合物形成的phaC1合酶的实时定量RT-PCR分析表明,野生型和gacS破坏菌株之间的转录水平没有统计学上的显着差异。随后,这些菌株的SDS-PAGE蛋白分析确定了phaC1合酶的转录后控制是恶臭假单胞菌CA-3调节PHA合成的关键方面。

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