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牲畜粪便沼气发酵过程中微生物丰度变化分析 被引量:2

Analysis on Abundance Changes of Microorganisms during Biogas Fermentation of Livestock Dung
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摘要 微生物在沼气发酵过程中起着重要的作用,采用实时荧光定量(quantitative real-time PCR,q PCR)技术检测了牲畜粪便沼气发酵过程中微生物的丰度变化。结果表明:夏季沼液样品中16S rRNA基因丰度从7.88×108copies/m L到6.35×1010copies/m L,平均为1.78×1010copies/m L,冬季沼液样品中16S rRNA基因丰度从4.04×108copies/m L到7.28×1010copies/m L,平均为1.89×1010copies/m L,而且新鲜猪粪、新鲜水牛粪及其混合物在发酵过程中其微生物丰度演变规律与其产气情况相一致。说明微生物在牲畜粪便沼气发酵过程决定着沼气发酵的产量和质量。 Microorganisms played critical roles in biogas fermentation. Abundance changes of microorganisms during biogas fermentation of livestock dung were tested by quantitative real-time PCR (qPCR). Results showed that the gene abundance of 16S rRNA in biogas liquid samples in summer ranged from 7.88 ×10^8 copies/mL to 6. 35×10^10 copies/mL, with an average of 1.78 ×10^10 copies/mL. The gene abundance of 16S rRNA in biogas liquid samples in winter ranged from 4. 04 ×10^8 copies/mL to 7.28×10^10 copies/mL, with an average of 1.89×10^10 copies/mL. The abundance change regularity of microorganisms during biogas fermentation of fresh pig dung, fresh cow dung and their mixtures was consist- ent with their biogas production performance, which indicated that microorganisms decided quantity and quality of biogas production in biogas fermentation of livestock dung.
出处 《广西林业科学》 2015年第4期416-420,共5页 Guangxi Forestry Science
基金 广西林科院基本科研业务费专项(林科201406号) 广西优良用材林资源培育重点实验室开放课题(13B0402) 广西科学研究与技术开发计划项目(桂科攻14124004-3-6)
关键词 沼气发酵 牲畜粪便 微生物丰度 实时荧光定量PCR biogas fermentation livestock dung abundance of microorganism quantitative realtime PCR
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  • 1Rozzi A,Remigi E.Methods of assessing microbial activity and inhibition under anaerobic contitions:a literature review[J].Reviews in Environmental Science and Bio/Technology,2004,3:93–115.
  • 2Traversi D,Capone C,Villa S,et al.Assessing archeal indicators of performance by RT-q PCR methods during anaerobic co-digestion of organic wastes[J].Bioenergy Research,2014,7:720–727.
  • 3张晶,张惠文,张成刚.实时荧光定量PCR及其在微生物生态学中的应用[J].生态学报,2005,25(6):1445-1450. 被引量:44
  • 4Smith C J,Osborn A M.Advantages and limitations of quantitative PCR(Q-PCR)-based approaches in microbial ecology[J].FEMS Microbiology Ecology,2009,67:6–20.
  • 5Coulson D T,Brockbank S,Quinn J G,et al.Identification of valid reference genes for the normalization of RT q PCR gene expression data in human brain tissue[J].BMC Molecular Biology,2008,9(18):1-11.
  • 6秦茜,郑美琴,汪盈,梁韶辉,诸葛青云.快速诊断早期棘阿米巴角膜炎qPCR方法的建立及应用[J].中国病原生物学杂志,2014,9(3):249-251. 被引量:3
  • 7Rademacher A,Zakrzewski M,Schluter A,et al.Characterization of microbial biofilms in a thermophilic biogas system by high-throughput metagenome sequencing[J].FEMS Microbiology Ecology,2012,79(3):785-799.
  • 8Walters W A,Caporaso J G,Lauber C L,et al.Primer prospector:de novo design and taxonomic analysis of barcoded polymerase chain reaction primers[J].Bioinformatics,2011,27(8):1159-1161.
  • 9Peiffer J A,Spor A,Koren O,et al.Diversity and heritability of the maize rhizosphere microbiome under field conditions[J].Proceedings of the National Academy of Sciences of the United States of America,2013,110(16):6548-6553.
  • 10Wang H Y,Tao Y,Temudo M,et al.Biomethanation from enzymatically hydrolyzed brewer’s spent grain:Impact of rapid increase in loadings[J].Bioresource Technology,2015,190:167–174.

二级参考文献63

  • 1单国彬,金文标,林佶侃,邢新会.变性梯度凝胶电泳在环境微生物生态学中的应用[J].生态学杂志,2006,25(10):1257-1264. 被引量:11
  • 2姬云丽.1994~2002年我国44例棘阿米巴角膜炎病例分析[J].中国寄生虫病防治杂志,2004,17(1):52-52. 被引量:4
  • 3吴彦萍,秦桂霞.棘阿米巴角膜炎22例报告[J].哈尔滨医药,2005,25(2):37-37. 被引量:3
  • 4朱学军,郑彩慧,韩晓丽,王晓辉,杨娟.棘阿米巴性角膜炎22例临床报告[J].海峡科学,2007(3):24-25. 被引量:3
  • 5Kolb S,Knief C,Stubner S,et al.Quantitative detection of methanotrophs in soil by novel pmoA-targeted real-time PCR assays.Applied and Environmental Microbiology,2003,69(5):2423~2429.
  • 6Tajima K,Aminov RI,Nagamine T,et al.Diet-dependent shift in the bacterial population of the rumen revealed with real-time PCR.Applied and Environmental Microbiology,2001,67(6):2766~2774.
  • 7Hristova K,Gebreyesus B,Mackay D,et al.Naturally occurring bacteria similar to the methyl tert-butyl ether (MTBE)-degrading strain PM1 are present in MTBE-contaminated groundwater.Applied and Environmental Microbiology,2003,69(5):2616~2623.
  • 8Boon N,Top EM,Verstraete W,et al.Bioaugmentation as a tool to protect the structure and function of an activated-sludge microbial community against a 3-chloroaniline shock load.Applied and Environmental Microbiology,2003,69(3):1511~1520.
  • 9Feris K,Ramsey P,Frazar C,et al.Differences in hyporheic-zone microbial community structure along a heavy-metal contamination gradient.Applied and Environmental Microbiology,2003,69(9):5563~5573.
  • 10Seghers D,Verthé K,Reheul D,et al.Effect of long-term herbicide applications on the bacterial community structure and function in an agricultural soil.FEMS Microbiology Ecology,2003,46:139~146.

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