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Biodegradation of 1-methylindole and 3-methylindole by mangrove sediment enrichment cultures and a pure culture of an isolated Pseudomonas aeruginosa Gs

机译:红树林沉积物富集培养物和分离的铜绿假单胞菌Gs的纯培养物生物降解1-甲基吲哚和3-甲基吲哚

摘要

Indolic compounds are N-heterocyclic aromatic chemicals and have been detected at contaminated sites. Biodegradation of 1-methylindole (1MI) and 3-methylindole (3MI) was investigated initially using enrichment cultures with mangrove sediment obtained from Mai Po Nature Reserve of Hong Kong and subsequently with a pure culture of Pseudomonas aeruginosa Gs confirmed with 16S rRNA gene. At 2.0 mM, 1MI and 3MI were degraded in 4 and 3 days, respectively, by the respective 1MI- and 3MI-degrading enrichment cultures. When substrate concentrations were increased to 3.0,mM and 3.5,mM, slower degradation of 1MI and 3MI was observed indicating inhibitory effects from the substrates, possibly due to toxicity. In addition, no colony of bacteria could be observed on the agar plates amended with 3.5,mM 1MI or 4.0,mM 3MI, indicating that 1MI was more toxic than 3MI. Pseudomonas aeruginosa Gs, isolated from the enrichment culture, effectively utilized both substrates as the sole source of carbon and energy. Complete degradation of 1MI and 3MI was achieved after more than 40 days and 24 days, respectively, at an initial concentration of 2,mM in the culture. Effects of initial substrate concentration, pH and salinity on degradation of 1MI and 3MI by P. aeruginosa Gs were also studied in batch culture. The optimum pH and salinity for degrading both substrates by P. aeruginosa Gs was 7.0 and 5‰, respectively. Biodegradation kinetics of 1MI and 3MI by P. aeruginosa Gs could be described using a first-order kinetic model. Our results suggest that both 1MI and 3MI are biodegradable in the mangrove environment and that toxicity of 1MI could be a potential factor limiting the removal of the chemical in the environment by microorganisms. © Springer 2006.
机译:吲哚化合物是N-杂环芳香族化学品,已在受污染的位置被发现。首先使用富集培养物(从香港米埔自然保护区获得的红树林沉积物),然后使用经16S rRNA基因确认的纯铜绿假单胞菌Gs培养,研究了1-甲基吲哚(1MI)和3-甲基吲哚(3MI)的生物降解。在2.0 mM下,分别降解1MI和3MI的富集培养物分别在4和3天内降解了1MI和3MI。当底物浓度增加到3.0,mM和3.5,mM时,观察到1MI和3MI的降解较慢,表明底物的抑制作用,可能是由于毒性。另外,在用3.5mM 1MI或4.0mM 3MI修饰的琼脂平板上未观察到细菌菌落,表明1MI比3MI毒性更大。从富集培养中分离出的铜绿假单胞菌Gs有效地利用了两种底物作为碳和能量的唯一来源。在培养液中初始浓度分别为2 mM时,分别超过40天和24天后,实现了1MI和3MI的完全降解。在分批培养中,还研究了初始底物浓度,pH和盐度对铜绿假单胞菌Gs降解1MI和3MI的影响。铜绿假单胞菌Gs降解两种底物的最佳pH和盐度分别为7.0和5‰。铜绿假单胞菌Gs对1MI和3MI的生物降解动力学可以用一级动力学模型来描述。我们的结果表明1MI和3MI在红树林环境中都是可生物降解的,并且1MI的毒性可能是限制微生物去除环境中化学物质的潜在因素。 ©Springer 2006。

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    Gu JD; Yin B; Huang L;

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  • 年度 2006
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  • 正文语种 eng
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