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Community and Proteomic Analysis of Methanogenic Consortia Degrading Terephthalate
Authors:Jer-Horng Wu  Feng-Yau Wu  Hui-Ping Chuang  Wei-Yu Chen  Hung-Jen Huang  Shu-Hui Chen  Wen-Tso Liu
Institution:aDepartment of Environmental Engineering, National Cheng Kung University, Taiwan, Republic of China;bDepartment of Chemistry, National Cheng Kung University, Taiwan, Republic of China;cDepartment of Civil and Environmental Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA
Abstract:Degradation of terephthalate (TA) through microbial syntrophy under moderately thermophilic (46 to 50°C) methanogenic conditions was characterized by using a metagenomic approach (A. Lykidis et al., ISME J. 5:122–130, 2011). To further study the activities of key microorganisms responsible for the TA degradation, community analysis and shotgun proteomics were used. The results of hierarchical oligonucleotide primer extension analysis of PCR-amplified 16S rRNA genes indicated that Pelotomaculum, Methanosaeta, and Methanolinea were predominant in the TA-degrading biofilms. Metaproteomic analysis identified a total of 482 proteins and revealed a distinctive distribution pattern of microbial functions expressed in situ. The results confirmed that TA was degraded by Pelotomaculum spp. via the proposed decarboxylation and benzoyl-coenzyme A-dependent pathway. The intermediate by-products, including acetate, H2/CO2, and butyrate, were produced to support the growth of methanogens, as well as other microbial populations that could further degrade butyrate. Proteins related to energy production and conservation, and signal transduction mechanisms (that is, chemotaxis, PAS/GGDEF regulators, and stress proteins) were highly expressed, and these mechanisms were important for growth in energy-limited syntrophic ecosystems.
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