Waller Alison S, Krajmalnik-Brown Rosa, Löffler Frank E, Edwards Elizabeth A
Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College St., Toronto, Ontario M5S 3E5, Canada.
Appl Environ Microbiol. 2005 Dec;71(12):8257-64. doi: 10.1128/AEM.71.12.8257-8264.2005.
Degenerate primers were used to amplify 14 distinct reductive-dehalogenase-homologous (RDH) genes from the Dehalococcoides-containing mixed culture KB1. Most of the corresponding predicted proteins were highly similar (97 to >99% amino acid identity) to previously reported Dehalococcoides reductive dehalogenases. To examine the differential transcription of these RDH genes, KB1 was split into five subcultures amended with either trichloroethene, cis-1,2-dichloroethene, vinyl chloride, 1,2-dichlorethane, or no chlorinated electron acceptor. Total RNA was extracted following the onset of reductive dechlorination, and RDH transcripts were reverse transcribed and amplified using degenerate primers. The results indicate that the transcription of RDH genes requires the presence of a chlorinated electron acceptor, and for all treatments, multiple RDH genes were simultaneously transcribed, with transcripts of two of the genes being present under all four electron-accepting conditions. Two of the transcribed sequences were highly similar to reported vinyl chloride reductase genes, namely, vcrA from Dehalococcoides sp. strain VS and bvcA from Dehalococcoides sp. strain BAV1. These findings suggest that multiple RDH genes are induced by a single chlorinated substrate and that multiple reductive dehalogenases contribute to chloroethene degradation in KB1.
利用简并引物从含有脱卤球菌的混合培养物KB1中扩增出14个不同的还原性脱卤酶同源(RDH)基因。大多数相应的预测蛋白与先前报道的脱卤球菌还原性脱卤酶高度相似(氨基酸同一性为97%至>99%)。为了检测这些RDH基因的差异转录,将KB1分成五个亚培养物,分别添加三氯乙烯、顺式-1,2-二氯乙烯、氯乙烯、1,2-二氯乙烷或不添加氯化电子受体。在还原性脱氯开始后提取总RNA,并用简并引物对RDH转录本进行逆转录和扩增。结果表明,RDH基因的转录需要氯化电子受体的存在,并且在所有处理中,多个RDH基因同时转录,其中两个基因的转录本在所有四种电子受体条件下均存在。两个转录序列与报道的氯乙烯还原酶基因高度相似,即脱卤球菌属菌株VS的vcrA和脱卤球菌属菌株BAV1的bvcA。这些发现表明,多个RDH基因由单一氯化底物诱导,并且多个还原性脱卤酶有助于KB1中氯乙烯的降解。