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Biodegradation of 2-chloro-4-nitrophenol via a hydroxyquinol pathway by a Gram-negative bacterium Cupriavidus sp. strain CNP-8

机译:革兰氏阴性菌Cupriavidus sp。通过羟基喹啉途径对2-氯-4-硝基苯酚进行生物降解。 CNP-8株

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摘要

Cupriavidus sp. strain CNP-8 isolated from a pesticide-contaminated soil was able to utilize 2-chloro-4-nitrophenol (2C4NP) as a sole source of carbon, nitrogen and energy, together with the release of nitrite and chloride ions. It could degrade 2C4NP at temperatures from 20 to 40 °C and at pH values from 5 to 10, and degrade 2C4NP as high as 1.6 mM. Kinetics assay showed that biodegradation of 2C4NP followed Haldane substrate inhibition model, with the maximum specific growth rate (μmax) of 0.148/h, half saturation constant (Ks) of 0.022 mM and substrate inhibition constant (Ki) of 0.72 mM. Strain CNP-8 was proposed to degrade 2C4NP with hydroxyquinol (1,2,4-benzenetriol, BT) as the ring-cleavage substrate. The 2C4NP catabolic pathway in strain CNP-8 is significant from those reported in other Gram-negative 2C4NP utilizers. Enzymatic assay indicated that the monooxygenase initiating 2C4NP catabolism had different substrates specificity compared with previously reported 2C4NP monooxygenations. Capillary assays showed that strain CNP-8 exhibited metabolism-dependent chemotactic response toward 2C4NP at the optimum concentration of 0.5 mM with a maximum chemotaxis index of 37.5. Furthermore, microcosm studies demonstrated that strain CNP-8, especially the pre-induced cells, could remove 2C4NP rapidly from the 2C4NP-contaminated soil. Considering its adaptability to pH and temperature fluctuations and great degradation efficiency against 2C4NP, strain CNP-8 could be a promising candidate for the bioremediation of 2C4NP-contaminated sites.Electronic supplementary materialThe online version of this article (10.1186/s13568-018-0574-7) contains supplementary material, which is available to authorized users.
机译:Cupriavidus sp。从受农药污染的土壤中分离出的CNP-8菌株能够利用2-氯-4-硝基苯酚(2C4NP)作为碳,氮和能量的唯一来源,同时释放出亚硝酸盐和氯离子。它可以在20至40°C的温度和5至10的pH值下降解2C4NP,并降解高达1.6mM的2C4NP。动力学分析表明2C4NP的生物降解遵循Haldane底物抑制模型,最大比生长速率(μmax)为0.148 / h,半饱和常数(Ks)为0.022 mM,底物抑制常数(Ki)为0.72 mM。有人提出用CNP-8菌株以羟喹醇(1,2,4-苯三醇,BT)为环裂解底物降解2C4NP。 CNP-8菌株中的2C4NP分解代谢途径与其他革兰氏阴性2C4NP利用者中报道的那些相当。酶法测定表明,与以前报道的2C4NP单加氧作用相比,引发2C4NP分解代谢的单加氧酶具有不同的底物特异性。毛细管测定表明,菌株CNP-8在最佳浓度为0.5mM时对2C4NP表现出依赖于代谢的趋化反应,最大趋化指数为37.5。此外,微观研究表明,菌株CNP-8,特别是预诱导的细胞,可以从受2C4NP污染的土壤中快速去除2C4NP。考虑到其对pH和温度波动的适应性以及对2C4NP的高降解效率,CNP-8菌株可能是2C4NP污染位点生物修复的有前途的候选者。电子补充材料本文的在线版本(10.1186 / s13568-018-0574- 7)包含补充材料,授权用户可以使用。

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