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Functional role of pyruvate kinase from Lactobacillus bulgaricus in acid tolerance and identification of its transcription factor by bacterial one-hybrid

机译:保加利亚乳杆菌丙酮酸激酶在耐酸中的功能及其细菌一杂交鉴定其转录因子的作用

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摘要

Lactobacillus delbrueckii subsp. bulgaricus develops acid tolerance response when subjected to acid stress conditions, such as the induction of enzymes associated with carbohydrate metabolism. In this study, pyk gene encoding pyruvate kinase was over-expressed in heterologous host Lactococcus lactis NZ9000, and SDS-PAGE analysis revealed the successful expression of this gene in NZ9000. The survival rate of Pyk-overproducing strain was 45-fold higher than the control under acid stress condition (pH 4.0). In order to determine the transcription factor (TF) which regulates the expression of pyk by bacterial one-hybrid, we constructed a TF library including 65 TFs of L. bulgaricus. Western blotting indicated that TFs in this library could be successfully expressed in host strains. Subsequently, the promoter of pfk-pyk operon in L. bulgaricus was identified by 5′-RACE PCR. The bait plasmid pH3U3-p01 carrying the deletion fragment of pfk-pyk promoter captured catabolite control protein A (CcpA) which could regulate the expression of pyk by binding to a putative catabolite-responsive element (5′-TGTAAGCCCTAACA-3′) upstream the -35 region. Real-time qPCR analysis revealed the transcription of pyk was positively regulated by CcpA. This is the first report about identifying the TF of pyk in L. bulgaricus, which will provide new insight into the regulatory network.
机译:德氏乳杆菌亚种。保加利亚人在遭受酸胁迫条件(例如诱导与碳水化合物代谢相关的酶)时会产生酸耐受性反应。在这项研究中,编码丙酮酸激酶的pyk基因在异源宿主乳酸乳球菌NZ9000中过表达,SDS-PAGE分析表明该基因在NZ9000中成功表达。在酸性胁迫条件下(pH 4.0),过量生产Pyk的菌株的存活率比对照高45倍。为了确定通过细菌单杂交调节pyk表达的转录因子(TF),我们构建了一个包含65个保加利亚乳杆菌TF的TF文库。蛋白质印迹表明该文库中的TFs可以在宿主菌株中成功表达。随后,通过5'-RACE PCR鉴定了保加利亚乳杆菌中pfk-pyk操纵子的启动子。携带pfk-pyk启动子缺失片段的诱饵质粒pH3U3-p01捕获了分解代谢物控制蛋白A(CcpA),该蛋白可通过与假定的分解代谢物响应元件(5'-TGTAAGCCCTAACA-3')结合来调节pyk的表达。 -35地区。实时qPCR分析显示pyk的转录受CcpA正调控。这是有关鉴定保加利亚乳杆菌中pyk TF的第一份报告,这将为监管网络提供新见解。

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