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基因组测序和比较转录组学提供了对菌株BUPNP1降解4-硝基苯酚及同时进行脂肪酸分解代谢的整体认识。

Genome Sequencing and Comparative Transcriptomics Provide a Holistic View of 4-Nitrophenol Degradation and Concurrent Fatty Acid Catabolism by sp. Strain BUPNP1.

作者信息

Sengupta Kriti, Swain Martin T, Livingstone Paul G, Whitworth David E, Saha Pradipta

机构信息

Department of Microbiology, Burdwan University, Bardhaman, India.

Institute of Biological, Environmental and Rural Sciences, Aberystwyth University, Aberystwyth, United Kingdom.

出版信息

Front Microbiol. 2019 Jan 4;9:3209. doi: 10.3389/fmicb.2018.03209. eCollection 2018.

Abstract

sp.strain BUPNP1 can utilize the priority environmental pollutant 4-nitrophenol (4-NP) as its sole source of carbon and energy. In this study, genome and transcriptome sequencing were used to gain mechanistic insights into 4-NP degradation. The draft BUPNP1 genome is 5.56 Mbp and encodes 4,963 proteins, which are significantly enriched in hypothetical proteins compared to other sp. A novel 4-NP catabolic 43 gene cluster "" was identified that encodes all the genes required for the conversion of 4-NP into acetyl-CoA and succinate, via 4-nitrocatechol. The cluster also encodes pathways for the catabolism of other diverse aromatic compounds. Comparisons between BUPN1 growing on either 4-NP or glucose resulted in significant changes in the expression of many cluster genes, and, during 4-NP growth, a loss of lipid inclusions. Moreover, fatty acid degradation/synthesis genes were found within the cluster, suggesting fatty acids may be concurrently catabolised with 4-NP. A holistic model for the action of the gene cluster is proposed which incorporates genetic architecture, uptake and metabolism of aromatic compounds, enzymatic activities and transcriptional regulation. The model provides testable hypotheses for further biochemical investigations into the genes of the cluster, for potential exploitation in bioremediation.

摘要

sp.菌株BUPNP1能够利用优先环境污染物4-硝基苯酚(4-NP)作为其唯一的碳源和能源。在本研究中,利用基因组和转录组测序来深入了解4-NP降解的机制。BUPNP1基因组草图为5.56 Mbp,编码4963种蛋白质,与其他sp.相比,这些蛋白质在假定蛋白质中显著富集。鉴定出一个新的4-NP分解代谢43基因簇,该基因簇编码将4-NP通过4-硝基邻苯二酚转化为乙酰辅酶A和琥珀酸所需的所有基因。该基因簇还编码其他多种芳香族化合物的分解代谢途径。在以4-NP或葡萄糖为生长底物的BUPN1之间进行比较,导致许多基因簇基因的表达发生显著变化,并且在4-NP生长期间,脂质内含物减少。此外,在基因簇内发现了脂肪酸降解/合成基因,表明脂肪酸可能与4-NP同时被分解代谢。提出了一个基因簇作用的整体模型,该模型整合了遗传结构、芳香族化合物的摄取和代谢、酶活性以及转录调控。该模型为进一步对基因簇基因进行生化研究提供了可检验的假设,以便在生物修复中进行潜在利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26aa/6328493/427e05c3f4bb/fmicb-09-03209-g0001.jpg

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