Identification of the green alga, Chlorella vulgaris (SDC1) using cyanobacteria derived 16S rDNA primers:: targeting the chloroplast

被引:26
作者
Burja, AM
Tamagnini, P
Bustard, MT
Wright, PC [1 ]
机构
[1] Heriot Watt Univ, Dept Mech & Chem Engn, Edinburgh EH14 4AS, Midlothian, Scotland
[2] Univ Porto, Dept Bot, Inst Mol & Cell Biol, P-4150180 Oporto, Portugal
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
bioinformatic; chloroplast; genomic; 16S rRNA gene fragment sequencing; green alga; Chlorella vulgaris;
D O I
10.1016/S0378-1097(01)00306-8
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have tested a set of oligonucleotide primers originally developed for the specific amplification of 16S rRNA gene segments from cyanobacteria, in order to determine their versatility as an identification tool for phototrophic eucaryotes. Using web-based bioinformatics tools we determined that these primers not only targeted cyanobacterium sequences as previously described, but also 87% of sequences derived from phototrophic eucaryotes. In order to qualify our finding, a type culture and environmental strain from the freshwater unicellular, green algae genus Chlorella Beijerinck, were selected for further study. Subsequently, we sequenced a 578-bp fragment of the 16S rRNA gene, which proved to be present within the chloroplast genome, performed sequence analysis and positively identified our solvent-degrading environmental strain (SDC1) as Chlorella vulgaris. (C) 2001 Published by Elsevier Science B.V. on behalf of the Federation of European Microbiological Societies.
引用
收藏
页码:195 / 203
页数:9
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