Department of Civil and Environmental Engineering, University of Iowa, Iowa City, IA, USA.
Environ Sci Technol. 2010 Mar 1;44(5):1594-601. doi: 10.1021/es903033r.
Contamination of groundwater with vinyl chloride (VC), a known human carcinogen, is a common environmental problem at plastics manufacturing, dry cleaning, and military sites. At many sites, there is the potential to cleanup VC groundwater plumes with aerobic VC-oxidizing microorganisms (e.g., methanotrophs, etheneotrophs, and VC-assimilating bacteria). Environmental biotechnologies that reveal the presence and activity of VC-oxidizing bacteria in contaminated groundwater samples would provide valuable lines of evidence that bioremediation of VC is occurring at a site. We applied targeted shotgun mass spectrometry-based proteomic methods to ethene-enriched groundwater microcosms from a VC-contaminated site. Polypeptides from the enzymes alkene monooxygenase (EtnC) and epoxyalkane:CoM transferase (EtnE), both of which are expressed by aerobic etheneotrophs and VC-assimilating bacteria, were identified in 7 of the 14 samples analyzed. Bioinformatic analysis revealed that 2 EtnC and 5 EtnE peptides were unique to deduced EtnC and EtnE sequences from two different cultivated strains. In addition, several partial EtnE genes sequenced from microcosms matched with observed EtnE peptides. Our results have revealed broader etheneotroph functional gene diversity and demonstrate the feasibility, speed, and accuracy of applying a targeted metaproteomics approach to identifying protein biomarkers from etheneotrophs in complex environmental samples.
地下水受到氯乙烯(VC)污染是塑料制造、干洗和军事场所等常见的环境问题,氯乙烯是一种已知的人类致癌物。在许多场地,利用好氧 VC 氧化微生物(如甲烷营养菌、乙烯营养菌和 VC 同化菌)来清理 VC 地下水羽流是有可能的。能够揭示污染地下水样本中 VC 氧化菌存在和活性的环境生物技术将提供宝贵的证据,证明该场地正在进行 VC 的生物修复。我们应用靶向 shotgun 基于质谱的蛋白质组学方法,对来自 VC 污染场地的富含乙烯的地下水微宇宙进行了分析。在分析的 14 个样本中的 7 个样本中,鉴定到了表达于好氧乙烯营养菌和 VC 同化菌的烯酶单加氧酶(EtnC)和环氧化物:CoM 转移酶(EtnE)的多肽。生物信息学分析表明,2 个 EtnC 和 5 个 EtnE 肽是从两种不同培养的菌株推断出的 EtnC 和 EtnE 序列所特有的。此外,从微宇宙中测序得到的几个部分 EtnE 基因与观察到的 EtnE 肽相匹配。我们的研究结果揭示了更广泛的乙烯营养菌功能基因多样性,并证明了应用靶向宏蛋白质组学方法从复杂环境样本中鉴定乙烯营养菌蛋白生物标志物的可行性、速度和准确性。