Yanagita K, Kamagata Y, Kawaharasaki M, Suzuki T, Nakamura Y, Minato H
National Institute of Bioscience and Human Technology, Agency of Industrial Science and Technology, Tsukuba, Ibaraki, Japan.
Biosci Biotechnol Biochem. 2000 Aug;64(8):1737-42. doi: 10.1271/bbb.64.1737.
The population of methanogens in the sheep rumen microbial ecosystem was studied by using 16S rDNA cloning analysis, epifluorescence microscopy (which detects autofluorescence of a specific cofactor F420 in methanogens) and the 16S rRNA-targeted in situ hybridization technique. The 16S rDNA clone libraries were constructed by PCR amplification with an Archaea-specific primer set and partial sequencing of the clonal 16S rDNAs was done. Phylogenetic analysis indicated that the clones were affiliated with Methanomicrobium ruminantium and mobile, Methanobrevibacter smithii. Epifluorescence microscopy (F420 autofluorescence) and in situ hybridization by using a newly designed M. mobile-specific 16S rRNA-targeted oligonucleotide probe found that methanogens accounted for approximately 3.6% of total ruminal microorganisms and approximately 54% of the total methanogens were M. mobile.
采用16S rDNA克隆分析、落射荧光显微镜技术(检测产甲烷菌中特定辅因子F420的自发荧光)和16S rRNA靶向原位杂交技术,对绵羊瘤胃微生物生态系统中产甲烷菌的种群进行了研究。通过使用古菌特异性引物对进行PCR扩增构建了16S rDNA克隆文库,并对克隆的16S rDNA进行了部分测序。系统发育分析表明,这些克隆与反刍甲烷微菌属和游动甲烷短杆菌相关。落射荧光显微镜技术(F420自发荧光)以及使用新设计的针对游动甲烷微菌的16S rRNA靶向寡核苷酸探针进行的原位杂交发现,产甲烷菌约占瘤胃微生物总数的3.6%,其中约54%的产甲烷菌为游动甲烷微菌。