Shin Eun Chule, Choi Byoung Rock, Lim Woo Jin, Hong Su Young, An Chang Long, Cho Kye Man, Kim Young Kyun, An Jin Mee, Kang Jung Mi, Lee Sung Sill, Kim Hoon, Yun Han Dae
Division of Applied Life Science, Research Institute of Life Science, Gyeongsang National University, Chinju 660-701, Republic of Korea.
Anaerobe. 2004 Dec;10(6):313-9. doi: 10.1016/j.anaerobe.2004.08.002.
Phylogenetic analysis of archaea in the rumen ecosystem was analysed by PCR of 16S rDNA from the bovine rumen using archaea-specific primers. The libraries were constructed from rumen fluid (AF), rumen solid (AS), and rumen epithelium (AE) from a rumen-fistulated Korean cow (Hanwoo). The 45 AF clones could be divided into three groups and the largest group was affiliated with the Methanomicrobiaceae family (96% of clones). The AF clones contained a high proportion of unidentifiable clones (67%). The 39 AE clones could be divided into two groups and the largest group was also affiliated with the Methanomicrobiaceae family (95% of clones). The AE clones contained a low proportion of unidentifiable clones (5%). The 20 AS clones could be divided into two groups that were affiliated with either the Methanobacteriaceae family (55%) or the Methanomicrobiaceae family (45%). The AS clones contained a moderate proportion of unidentifiable clones (40%). The predominant family of whole rumen archaea was found to belong to the Methanomicrobiaceae (85%). Methanomicrobiaceae were predominant in the rumen epithelium and the rumen fluid while Methanobacteriaceae were predominant in the rumen solid. One clone from the rumen fluid and two clones from the rumen epithelium contained rDNA sequences of Non-Thermophilic-Crenarchaeota (NTC) and Thermophilic-Crenarchaeota (TC), respectively, which have not previously been described from the rumen.
利用古菌特异性引物,通过对来自牛瘤胃的16S rDNA进行PCR扩增,分析瘤胃生态系统中古菌的系统发育。文库由一头瘤胃造瘘的韩国牛(韩牛)的瘤胃液(AF)、瘤胃固体(AS)和瘤胃上皮(AE)构建而成。45个AF克隆可分为三组,最大的一组隶属于甲烷微菌科(占克隆的96%)。AF克隆中不可识别克隆的比例较高(67%)。39个AE克隆可分为两组,最大的一组也隶属于甲烷微菌科(占克隆的95%)。AE克隆中不可识别克隆的比例较低(5%)。20个AS克隆可分为两组,分别隶属于甲烷杆菌科(55%)或甲烷微菌科(45%)。AS克隆中不可识别克隆的比例适中(40%)。发现整个瘤胃古菌的优势科属于甲烷微菌科(85%)。甲烷微菌科在瘤胃上皮和瘤胃液中占主导地位,而甲烷杆菌科在瘤胃固体中占主导地位。来自瘤胃液的一个克隆和来自瘤胃上皮的两个克隆分别含有非嗜热泉古菌(NTC)和嗜热泉古菌(TC)的rDNA序列,此前在瘤胃中尚未有过描述。