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首页> 外文期刊>Applied Microbiology and Biotechnology >A sirA-like gene, sirA2, is essential for 3-succinoyl-pyridine metabolism in the newly isolated nicotine-degrading Pseudomonas sp. HZN6 strain
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A sirA-like gene, sirA2, is essential for 3-succinoyl-pyridine metabolism in the newly isolated nicotine-degrading Pseudomonas sp. HZN6 strain

机译:sirA样基因sirA2对于新分离的可降解烟碱的假单胞菌sp-3-琥珀酰-吡啶代谢至关重要。 HZN6株

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A novel nicotine-degrading Pseudomonas sp. strain, HZN6, was isolated from a pesticide-wastewater treatment facility in Hangzhou. The strain could grow on nicotine as its sole source of carbon, nitrogen, and energy. The strain's main intermediate metabolites were determined to be pseudooxynicotine, 3-succinoyl-pyridine (SP), and 6-hydroxy-3-succinoyl-pyridine (HSP). A Tn5 transposon mutant was generated in which the degradation pathway was blocked at the SP. A 4,583-bp DNA fragment flanking the transposon insertion site was obtained through self-formed adaptor PCR and analyzed. The mutant gene orfC displays 89% deduced amino acid sequence identity with the sirA-like gene (sirA2, a sulfurtransferase homologue gene) of Pseudomonas stutzeri A1501. The orfC-disrupted strain lost the ability to degrade SP, and the complementation strains with the orfC from the Pseudomonas sp. HZN6 and the sirA2 (PP-1233) from Pseudomonas putida KT2440 recovered the degradation ability. Though the orfC-disrupted strain also lost the xanthine dehydrogenase activity, the effects of tungsten on the degradation of SP and hypoxanthine revealed that the hydroxylation of SP to HSP was not a xanthine dehydrogenase type. These results demonstrated that the orfC gene was essential for the SP metabolism involved in the nicotine metabolic pathway in the Pseudomonas sp. HZN6 strain. This study might advance the understanding of the nicotine metabolic mechanism in Pseudomonas.
机译:一种新型的尼古丁降解假单胞菌。 HZN6菌株是从杭州的一家农药废水处理厂中分离出来的。该菌株可以在尼古丁上生长,这是其唯一的碳,氮和能量来源。该菌株的主要中间代谢产物被确定为拟氧烟碱,3-琥珀酰-吡啶(SP)和6-羟基-3-琥珀酰-吡啶(HSP)。生成了一个Tn5转座子突变体,其中降解途径在SP处被阻断。通过自形成的衔接子PCR获得了一个4,583-bp的DNA片段,位于转座子插入位点的两侧。突变基因orfC与斯图氏假单胞菌A1501的sirA样基因(sirA2,硫转移酶同源基因)显示了89%的推导氨基酸序列同一性。破坏orfC的菌株失去了降解SP的能力,与假单胞菌sp。的orfC互补的菌株也丧失了。恶臭假单胞菌KT2440的HZN6和sirA2(PP-1233)恢复了降解能力。尽管破坏了orfC的菌株也失去了黄嘌呤脱氢酶的活性,但钨对SP和次黄嘌呤降解的影响表明,SP向HSP的羟基化不是黄嘌呤脱氢酶类型。这些结果表明,orfC基因对于假单胞菌属物种烟碱代谢途径中的SP代谢至关重要。 HZN6株。这项研究可能会增进对假单胞菌中尼古丁代谢机制的了解。

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