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首页> 外文期刊>Biodegradation >Characterization of a para-nitrophenol catabolic cluster in Pseudomonas sp strain NyZ402 and construction of an engineered strain capable of simultaneously mineralizing both para- and ortho-nitrophenols
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Characterization of a para-nitrophenol catabolic cluster in Pseudomonas sp strain NyZ402 and construction of an engineered strain capable of simultaneously mineralizing both para- and ortho-nitrophenols

机译:假单胞菌NyZ402菌株中对硝基苯酚分解代谢簇的表征和能够同时矿化对硝基和邻硝基苯酚的工程菌株的构建

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摘要

Pseudomonas sp. strain NyZ402 was isolated for its ability to grow on para-nitrophenol (PNP) as a sole source of carbon, nitrogen, and energy, and was shown to degrade PNP via an oxidization pathway. This strain was also capable of growing on hydroquinone or catechol. A 15, 818 bp DNA fragment extending from a 800-bp DNA fragment of hydroxyquinol 1,2-dioxygenase gene (pnpG) was obtained by genome walking. Sequence analysis indicated that the PNP catabolic gene cluster (pnpABCDEFG) in this fragment shared significant similarities with a recently reported gene cluster responsible for PNP degradation from Pseudomonas sp. strain WBC-3. PnpA is PNP 4-monooxygenase converting PNP to hydroquinone via benzoquinone in the presence of NADPH, and genetic analysis indicated that pnpA plays a key role in PNP degradation. pnpA1 present in the upstream of the cluster (absent in the cluster from strain WBC-3) encodes a protein sharing as high as 55% identity with PnpA, but was not involved in PNP degradation by either in vitro or in vivo analyses. Furthermore, an engineered strain capable of growing on PNP and ortho-nitrophenol (ONP) was constructed by introducing onpAB (encoding ONP monooxygenase and ortho-benzoquinone reductase which catalyzed the transformation of ONP to catechol) from Alcaligenes sp. strain NyZ215 into strain NyZ402.
机译:假单胞菌NyZ402菌株因其在对硝基苯酚(PNP)上作为碳,氮和能量的唯一来源而生长的能力而被分离,并显示可通过氧化途径降解PNP。该菌株也能够在对苯二酚或邻苯二酚上生长。通过基因组步移获得从羟基喹啉1,2-双加氧酶基因(pnpG)的800bp DNA片段延伸的15,818bp DNA片段。序列分析表明,该片段中的PNP分解代谢基因簇(pnpABCDEFG)与最近报道的负责Pseudomonas sp降解PNP的基因簇具有显着相似性。菌株WBC-3。 PnpA是在NADPH存在下通过苯醌将PNP转化为对苯二酚的PNP 4-单加氧酶,遗传分析表明pnpA在PNP降解中起关键作用。存在于簇上游(菌株WBC-3的簇中不存在)的pnpA1编码与PnpA共享高达55%的同一性的蛋白,但通过体外或体内分析均不参与PNP降解。此外,通过从Alcaligenes sp。导入onpAB(编码ONP单加氧酶和邻苯二酚还原酶,催化ONP向邻苯二酚的转化),构建了能够在PNP和邻硝基苯酚(ONP)上生长的工程菌株。菌株NyZ215转化为菌株NyZ402。

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