Lee T J, Kawaharasaki M, Matsumura M, Nakamura K
Institute of Applied Biochemistry, University of Tsukuba, Ibaraki, Japan.
Environ Technol. 2002 Jul;23(7):747-55. doi: 10.1080/09593332308618371.
The microbial community structures of anaerobic-aerobic activated sludges, which are dominated with polyphosphate-accumulating bacteria (PABs) and glycogen-accumulating bacteria (GABs), were investigated by quinone profile method and dual staining DAPI (4',6-diamidino-2-phenylindol dihydrochloride) with fluorescent in situ hybridization (FISH). For both activated sludges, the predominant bacterial groups were the beta subclass of the Proteobacteria that contained mainly Q-8 as analyzed by the quinone profile method and gram-positive bacteria with a high DNA G+C content based on FISH. A 16S rRNA-targeted oligonucleotide probe (MP2) specific for M. phosphovorus, a known polyphosphate-accumulating bacterium, was also applied to PABs and GABs-enriched activated sludge to evaluate their possible role in the enhanced biological phosphorus removal (EBPR) process. Interestingly, the bacteria that hybridized with the probe specific to M. phosphovorus in the sludge dominated with PABs represent about 6.9% of the total microorganisms. In the sludge dominated with GABs, these bacteria were about 1.9%. These results suggest its possible involvement in the EBPR process.
采用醌谱法以及4',6-二脒基-2-苯基吲哚二盐酸盐(DAPI)双重染色结合荧光原位杂交(FISH)技术,对以聚磷菌(PABs)和糖原积累菌(GABs)为主的厌氧-好氧活性污泥的微生物群落结构进行了研究。对于这两种活性污泥,通过醌谱法分析,主要细菌类群为变形菌门的β亚类,其主要含有Q-8;基于FISH技术,主要细菌类群为DNA G+C含量高的革兰氏阳性菌。一种针对已知聚磷菌——聚磷莫拉菌(M. phosphovorus)的16S rRNA靶向寡核苷酸探针(MP2),也被应用于富含PABs和GABs的活性污泥中,以评估它们在强化生物除磷(EBPR)过程中的可能作用。有趣的是,在以PABs为主的污泥中,与聚磷莫拉菌特异性探针杂交的细菌约占微生物总数的6.9%。在以GABs为主的污泥中,这些细菌约占1.9%。这些结果表明其可能参与了EBPR过程。