Mattes Timothy E, Coleman Nicholas V, Chuang Adina S, Rogers Andrea J, Spain Jim C, Gossett James M
Department of Civil and Environmental Engineering, 4105 Seamans Center, The University of Iowa, Iowa City, IA 52242, USA.
Arch Microbiol. 2007 Mar;187(3):217-26. doi: 10.1007/s00203-006-0189-2. Epub 2006 Nov 25.
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.
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。