Kühner Simon, Wöhlbrand Lars, Fritz Ingo, Wruck Wasco, Hultschig Claus, Hufnagel Peter, Kube Michael, Reinhardt Richard, Rabus Ralf
Max Planck Institute for Marine Microbiology, Celsiusstr. 1, 28359 Bremen, Germany.
J Bacteriol. 2005 Feb;187(4):1493-503. doi: 10.1128/JB.187.4.1493-1503.2005.
Anaerobic biodegradation of toluene and ethylbenzene is of environmental concern and biochemical interest due to toxicity and novel reactions, respectively. The denitrifying strain EbN1 is unique in anaerobically degrading both alkylbenzenes via different pathways which converge at benzoyl coenzyme A. The organization of genes involved in both pathways was only recently determined for strain EbN1. In the present study, global expression analysis (DNA microarray and proteomics) indicated involvement of several thus-far-unknown proteins in the degradation of both alkylbenzenes. For example, orf68 and orf57, framing the ebd operon, are implicated in ethylbenzene degradation, and the ebA1932 and ebA1936 genes, located 7.2 kb upstream of the bbs operon, are implicated in toluene degradation. In addition, expression studies were now possible on the level of the complete pathways. Growth experiments demonstrated that degradative capacities for toluene and ethylbenzene could be simultaneously induced, regardless of the substrate used for adaptation. Regulation was studied at the RNA (real-time reverse transcription-PCR and DNA microarray) and protein (two-dimensional-difference gel electrophoresis) level by using cells adapted to anaerobic growth with benzoate, toluene, ethylbenzene, or a mixture of toluene and ethylbenzene. Expression of the two toluene-related operons (bss and bbs) was specifically induced in toluene-adapted cells. In contrast, genes involved in anaerobic ethylbenzene degradation were induced in ethylbenzene- and toluene-adapted cells, suggesting that toluene may act as a gratuitous inducer. In agreement with the predicted sequential regulation of the ethylbenzene pathway, Ebd proteins (encoding subunits of ethylbenzene dehydrogenase) were formed in ethylbenzene- but not in acetophenone-adapted cells, while Apc proteins (subunits of predicted acetophenone carboxylase) were formed under both conditions.
甲苯和乙苯的厌氧生物降解分别因其毒性和新颖反应而受到环境关注和具有生化研究意义。反硝化菌株EbN1在通过不同途径厌氧降解这两种烷基苯方面具有独特性,这两条途径在苯甲酰辅酶A处汇合。参与这两条途径的基因组织直到最近才在菌株EbN1中确定。在本研究中,全局表达分析(DNA微阵列和蛋白质组学)表明,几种迄今未知的蛋白质参与了这两种烷基苯的降解。例如,位于ebd操纵子两侧的orf68和orf57与乙苯降解有关,位于bbs操纵子上游7.2 kb处的ebA1932和ebA1936基因与甲苯降解有关。此外,现在可以在完整途径水平上进行表达研究。生长实验表明,无论用于适应性培养的底物是什么,甲苯和乙苯的降解能力都可以同时被诱导。通过使用适应于以苯甲酸盐、甲苯、乙苯或甲苯和乙苯混合物进行厌氧生长的细胞,在RNA(实时逆转录PCR和DNA微阵列)和蛋白质(二维差异凝胶电泳)水平上研究了调控情况。两个与甲苯相关的操纵子(bss和bbs)的表达在适应甲苯的细胞中被特异性诱导。相反,参与厌氧乙苯降解的基因在适应乙苯和甲苯的细胞中被诱导,这表明甲苯可能作为一种 gratuitous 诱导剂。与乙苯途径的预测顺序调控一致,Ebd蛋白(编码乙苯脱氢酶的亚基)在适应乙苯的细胞中形成,而在适应苯乙酮的细胞中不形成,而Apc蛋白(预测的苯乙酮羧化酶的亚基)在两种条件下都形成。