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Microbial cycling of isoprene the most abundantly produced biological volatile organic compound on Earth

机译:异戊二烯的微生物循环异戊二烯是地球上生产最丰富的生物挥发性有机化合物

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摘要

Isoprene (2-methyl-1,3-butadiene), the most abundantly produced biogenic volatile organic compound (BVOC) on Earth, is highly reactive and can have diverse and often detrimental atmospheric effects, which impact on climate and health. Most isoprene is produced by terrestrial plants, but (micro)algal production is important in aquatic environments, and the relative bacterial contribution remains unknown. Soils are a sink for isoprene, and bacteria that can use isoprene as a carbon and energy source have been cultivated and also identified using cultivation-independent methods from soils, leaves and coastal/marine environments. Bacteria belonging to the Actinobacteria are most frequently isolated and identified, and Proteobacteria have also been shown to degrade isoprene. In the freshwater-sediment isolate, Rhodococcus strain AD45, initial oxidation of isoprene to 1,2-epoxy-isoprene is catalyzed by a multicomponent isoprene monooxygenase encoded by the genes isoABCDEF. The resultant epoxide is converted to a glutathione conjugate by a glutathione S-transferase encoded by isoI, and further degraded by enzymes encoded by isoGHJ. Genome sequence analysis of actinobacterial isolates belonging to the genera Rhodococcus, Mycobacterium and Gordonia has revealed that isoABCDEF and isoGHIJ are linked in an operon, either on a plasmid or the chromosome. In Rhodococcus strain AD45 both isoprene and epoxy-isoprene induce a high level of transcription of 22 contiguous genes, including isoABCDEF and isoGHIJ. Sequence analysis of the isoA gene, encoding the large subunit of the oxygenase component of isoprene monooxygenase, from isolates has facilitated the development of PCR primers that are proving valuable in investigating the ecology of uncultivated isoprene-degrading bacteria.
机译:异戊二烯(2-甲基-1,3-丁二烯)是地球上生产最丰富的生物挥发性有机化合物(BVOC),具有很高的反应活性,并且可能具有多种多样的有害空气效应,从而影响气候和健康。大多数异戊二烯是由陆生植物生产的,但是在水生环境中,(微)藻类的生产很重要,相对细菌的贡献仍然未知。土壤是异戊二烯的汇,已经培养了可以使用异戊二烯作为碳和能源的细菌,并使用了与栽培无关的方法从土壤,树叶和沿海/海洋环境中进行了鉴定。属于放线菌的细菌是最常分离和鉴定的,并且也已证明变形杆菌会降解异戊二烯。在淡水沉积物分离株(红球菌AD45)中,异戊二烯初始氧化为1,2-环氧异戊二烯是由isoABCDEF基因编码的多组分异戊二烯单加氧酶催化的。所得的环氧化物通过由isoI编码的谷胱甘肽S-转移酶转化为谷胱甘肽共轭物,并进一步由isoGHJ编码的酶降解。属于红球菌属,分枝杆菌属和戈多尼亚属的放线菌分离株的基因组序列分析表明,isoABCDEF和isoGHIJ在操纵子中相连,要么在质粒上,要么​​在染色体上。在红球菌菌株AD45中,异戊二烯和环氧异戊二烯均诱导22个连续基因(包括isoABCDEF和isoGHIJ)的高水平转录。从分离物中对编码异戊二烯单加氧酶加氧酶成分的大亚基的isoA基因进行序列分析,促进了PCR引物的开发,这些引物被证明对研究未培养的异戊二烯降解细菌的生态学非常有价值。

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