| Literature DB >> 26573961 |
Yaohui Wang1, Caina Jiang1, Guiqing Wen1, Xinghui Zhang1, Yanghe Luo1, Aimiao Qin1, Aihui Liang1, Zhiliang Jiang1.
Abstract
Negatively charged bacteria combined with positively charged alkaline dye rhodamine 6G (Rh6G) in NaH2 PO4 -Na2 HPO4 buffer solution pH 7.4, by electrostatic interaction. The dyed bacteria exhibited a strong fluorescence peak at 552 nm and fluorescence intensity was directly linear to Escherichia coli (E. coli), Bacillus subtilis (B. subtilis) and Staphylococcus aureus (S. aureus) concentrations in the range of 7.06 × 10(4) to 3.53 × 10(7) , 4.95 × 10(5) to 2.475 × 10(8) and 32.5 to 16250 colony forming unit/mL (cfu/mL) respectively, with detection limits of 3.2 × 10(4) cfu/mL E. coli, 2.3 × 10(5) cfu/mL B. subtilis and 16 cfu/mL S. aureus, respectively. Samples were cultured for 12 h, after which the linear detection range for E. coli was 2 to 88 cfu/mL. This simple, rapid and sensitive method was used for the analysis of water and drinking samples.Entities:
Keywords: E. coli; Rh6G, dying; fluorescence analysis
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Year: 2015 PMID: 26573961 DOI: 10.1002/bio.3060
Source DB: PubMed Journal: Luminescence ISSN: 1522-7235 Impact factor: 2.464