Rheims H, Felske A, Seufert S, Stackebrandt E
DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Braunschweig, Germany.
J Microbiol Methods. 1999 May;36(1-2):65-75. doi: 10.1016/s0167-7012(99)00012-3.
Previous investigations of 16S rRNA clone libraries from a wide spectrum of mainly terrestrial origin have shown the worldwide distribution of several as yet uncultivated phylogenetically deeply rooting groups of Actinobacteria. From the percentage of the occurrence of these clones it was concluded that these organisms constitute a significant part of the bacterial microflora in these habitats. Two of the clone groups, previously designated group II and group III, were shown to be phylogenetically moderately related among each other. In order to more exactly determine the abundance of a representative of group II, clone DA079, the fraction of the organism's rRNA in total extracted rRNA was determined in several neighboring samples from Drentse A grassland soil (The Netherlands). The fraction ranged from 2.6 to 9.1%, averaging 5.5%. Based upon comparison of total rRNA and strain DA079-specific rRNA it was concluded that on the average 2 x 10(6) cells/g of this organism are present in the investigated soil. Attempts to isolate members of one of the 16S rDNA clone groups of Actinobacteria were made with samples from a German peat bog, in which the organisms had been detected previously. Molecular detection of group III organisms by a nested PCR approach was possible in different cultivation media. Despite the wide spectrum of growth media employed the isolation of group III strains failed.
此前对大量主要来源于陆地的16S rRNA克隆文库的研究表明,几种尚未培养的系统发育上根深蒂固的放线菌菌群在全球范围内分布。从这些克隆出现的百分比可以得出结论,这些生物体构成了这些栖息地细菌微生物群落的重要组成部分。其中两个克隆组,之前分别命名为第二组和第三组,在系统发育上彼此有中等程度的相关性。为了更准确地确定第二组的一个代表克隆DA079的丰度,在来自荷兰德伦特省A草原土壤的几个相邻样本中测定了该生物体rRNA在总提取rRNA中的比例。该比例范围为2.6%至9.1%,平均为5.5%。基于总rRNA与菌株DA079特异性rRNA的比较得出结论,在所研究的土壤中平均每克有2×10⁶个这种生物体的细胞。人们尝试从德国泥炭沼泽的样本中分离放线菌16S rDNA克隆组之一的成员,此前在该泥炭沼泽中已检测到这些生物体。通过巢式PCR方法在不同的培养基中对第三组生物体进行分子检测是可行的。尽管使用了多种生长培养基,但第三组菌株的分离仍未成功。