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控制诺卡氏菌属菌株JS614中与氯乙烯饥饿相关的延长延迟期的机制。

Mechanism controlling the extended lag period associated with vinyl chloride starvation in Nocardioides sp. strain JS614.

作者信息

Mattes Timothy E, Coleman Nicholas V, Chuang Adina S, Rogers Andrea J, Spain Jim C, Gossett James M

机构信息

Department of Civil and Environmental Engineering, 4105 Seamans Center, The University of Iowa, Iowa City, IA 52242, USA.

出版信息

Arch Microbiol. 2007 Mar;187(3):217-26. doi: 10.1007/s00203-006-0189-2. Epub 2006 Nov 25.

Abstract

The extended lag period associated with vinyl chloride (VC) starvation in VC- and ethene-assimilating Nocardioides sp. strain JS614 was examined. The extended lag periods were variable (3-7 days), only associated with growth on VC or ethene, and were observed in VC- or ethene-grown cultures following 24 h carbon starvation and mid-exponential phase cultures grown on non-alkene carbon sources (e.g. acetate). Alkene monooxygenase (AkMO) and epoxyalkane:coenzyme M transferase (EaCoMT) are the initial enzymes of VC and ethene biodegradation in strain JS614. Reverse-transcription PCR confirmed that the AkMO gene etnC was expressed in response to epoxyethane, a metabolic intermediate of ethene biodegradation. Epoxyethane (0.5 mM) eliminated the extended lag period in both starved and mid-exponential phase cultures, suggesting that epoxyethane accumulation activates AkMO expression in strain JS614. AkMO activity in ethene-grown cultures was not detected after 6.7 h of carbon starvation, while 40% of the initial EaCoMT activity remained after 24 h. Acetate eliminated the extended lag period in starved cultures but not in mid-exponential phase cultures suggesting that acetate reactivates extant AkMO in starved VC- or ethene-grown cultures. The imbalance between AkMO and EaCoMT activities during starvation likely contributes to the extended lag period by delaying epoxide accumulation and subsequent AkMO induction.

摘要

对能同化氯乙烯(VC)和乙烯的诺卡氏菌属菌株JS614中与氯乙烯饥饿相关的延长滞后期进行了研究。延长滞后期是可变的(3 - 7天),仅与在VC或乙烯上的生长有关,并且在24小时碳饥饿后的VC或乙烯培养物以及在非烯烃碳源(如乙酸盐)上生长的指数中期培养物中观察到。烯烃单加氧酶(AkMO)和环氧烷:辅酶M转移酶(EaCoMT)是菌株JS614中VC和乙烯生物降解的初始酶。逆转录PCR证实,AkMO基因etnC响应环氧乙烷(乙烯生物降解的代谢中间体)而表达。环氧乙烷(0.5 mM)消除了饥饿和指数中期培养物中的延长滞后期,表明环氧乙烷的积累激活了菌株JS614中AkMO的表达。在碳饥饿6.7小时后,未检测到乙烯培养物中的AkMO活性,而24小时后仍保留40%的初始EaCoMT活性。乙酸盐消除了饥饿培养物中的延长滞后期,但未消除指数中期培养物中的延长滞后期,这表明乙酸盐在饥饿的VC或乙烯培养物中重新激活了现存的AkMO。饥饿期间AkMO和EaCoMT活性之间的不平衡可能通过延迟环氧化物积累和随后的AkMO诱导而导致延长滞后期。

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