Department of Life Sciences, Trent Polytechnic, Nottingham, Celltech Ltd., Slough SL1 4DY, Berkshire, and ICI Petrochemicals and Plastics Division, Wilton, Cleveland, England.
Appl Environ Microbiol. 1985 May;49(5):1282-9. doi: 10.1128/aem.49.5.1282-1289.1985.
An unusual Xanthobacter sp., capable of independent growth on cyclohexane as the sole source of carbon and energy, has been isolated from soil by using classical enrichment techniques. The mean generation time for growth on cyclohexane was 6 h. The microorganism showed a limited ability to utilize hydrocarbons, with only alicyclic hydrocarbons closely related to cyclohexane supporting growth. Ultrastructural studies indicated the presence of electron-transparent vesicles in the cyclohexane-grown Xanthobacter sp., but the presence of complex intracytoplasmic membranes could not be identified. A soluble inducible enzyme capable of oxidizing cyclohexane was identified in cell extracts. This enzyme had a pH optimum of 6.5, an absolute specificity for NADPH, and a stoichiometric requirement for molecular O(2) which was consistent with the formation of cyclohexanol. The enzyme showed no activity towards straight chain alkanes and only a limited activity towards unsaturated ring compounds. Enzymatic studies with cell extracts have indicated the main route of metabolism of cyclohexane by this Xanthobacter sp. to proceed via cyclohexane --> cyclohexanol --> cyclohexanone --> 1-oxa-2-oxocycloheptane (epsilon-caprolactone) --> 6-hydroxyhexanoate (6-hydroxycaproate) --> --> adipic acid. Alternative routes involving initial double hydroxylation of the cyclohexane ring may operate fortuituously but are unlikely to represent major pathways for the dissimilation of cyclohexane by this microorganism.
一株能够以环己烷作为唯一碳源和能源进行独立生长的罕见黄杆菌(Xanthobacter),通过使用经典的富集技术从土壤中分离得到。该微生物在环己烷上的平均世代时间为 6 小时。该微生物利用烃类的能力有限,只有与环己烷密切相关的脂环烃才能支持其生长。超微结构研究表明,在环己烷生长的黄杆菌中存在电子透明小泡,但不能确定是否存在复杂的胞内膜。在细胞提取物中鉴定出一种能够氧化环己烷的可诱导可溶性酶。该酶的 pH 最适值为 6.5,对 NADPH 具有绝对特异性,并且对分子 O(2)的需求呈计量关系,这与环己醇的形成一致。该酶对直链烷烃没有活性,对不饱和环化合物的活性也有限。细胞提取物的酶学研究表明,该黄杆菌代谢环己烷的主要途径是通过环己烷 --> 环己醇 --> 环己酮 --> 1-氧代-2-氧代环己烷(ε-己内酯)--> 6-羟基己酸(6-羟基己酸)--> --> 己二酸。初始环己烷环的双羟化作用可能偶然发生,但不太可能是该微生物异化环己烷的主要途径。