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Specific and sensitive detection of Alcaligenes species from an agricultural environment
Authors:Miyo Nakano  Masumi Niwa  Norihiro Nishimura
Institution:1. Department of Translational Medical Science and Molecular and Cellular Pharmacology, Pharmacogenomics, and Pharmacoinformatics, Mie University Graduate School of Medicine, Mie University, , 2‐174 Edobashi, Tsu, Mie 514‐8507, Japan;2. Designerfoods. Co., Ltd., NALIC207, Chikusa 2‐22‐8, , Chikusa‐ku, Nagoya, Aichi, 464‐0858, Japan
Abstract:A quantitative real‐time PCR assay to specifically detect and quantify the genus Alcaligenes in samples from the agricultural environment, such as vegetables and farming soils, was developed. The minimum detection sensitivity was 106 fg of pure culture DNA, corresponding to DNA extracted from two cells of Alcaligenes faecalis. To evaluate the detection limit of A. faecalis, serially diluted genomic DNA from this organism was mixed with DNA extracted from soil and vegetables and then a standard curve was constructed. It was found that Alcaligenes species are present in the plant phytosphere at levels 102–104 times lower than those in soil. The approach presented here will be useful for tracking or quantifying species of the genus Alcaligenes in the agricultural environment.
Keywords:16S rRNA  Alcaligenes species  plant phylloepiphytic bacteria  real‐time polymerase chain reaction
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