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首页> 外文期刊>Communications in Agricultural and Applied Biological Sciences >IDENTIFICATION OF BACTERIAL CANKER CAUSED BY PSEUDOMONAS SYRINGAE PV. SYRINGAEON SWEET CHERRY TREES IN TEKIRDAG
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IDENTIFICATION OF BACTERIAL CANKER CAUSED BY PSEUDOMONAS SYRINGAE PV. SYRINGAEON SWEET CHERRY TREES IN TEKIRDAG

机译:鉴定鉴定鉴定副癌胶印引起的乳酸染素PV。 在tekirdag的甜樱桃树

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摘要

Sweet cherry (Prunus avium L.) is one of the most important fruit trees grown in Tekirdag. Bacterial canker, which reduces the yield and quality of sweet cherry fruit and causes death of trees, was investigated. For this purpose, a survey study was conducted in 2012-2013, and 129 plant tissue samples were collected from symptomatic trees. Forty-one isolates from naturally infected plants were isolated and subjected to biochemical and pathogenicity tests. All strains were fluorescent on KB. On KB medium, most of the isolates produced slowly growing small, greyish-white colonies as reported previously (Lelliott and Stead, 1987). The reaction of P. syringae pv. syringae strains was positive for levan production; hypersensitive reaction on tobacco, gelatin hydrolysis, aesculine hydrolysis and negative for oxidase reaction, pectinolytic activity, arginine dehydrolase, tyrosine, tartaric acid. PCR studies were performed in a thermal cycler using primers, Bl (5'-CTTTCCGTGGTCTTGATGAGG- 3')-B2 (5'-TCGATTTT-GCCGTGATGAGTC- 3') specific for P. syringae pv. syringae for amplification of 752 bp of the syrB gene. In total, 41 bacterial strains of Pseudomonas syringae were determined by using classical and molecular identification tests, 18 strain were identifiedas Pseudomonas syringae pv. syringae.
机译:甜樱桃(Prunus Avium L.)是Tekirdag中种植的最重要的果树之一。调查了细菌溃疡,降低了甜樱桃果实的产量和质量,并导致树木死亡。为此,在2012 - 2013年进行了调查研究,并从症状树木中收集了129种植物组织样本。分离出自然感染植物的四十一体分离物并进行生化和致病性试验。所有菌株都在KB上荧光。在KB培养基上,大多数分离物在此前报道的(Lelliott and Stead,1987)所报道的那样产生慢慢生长的小,灰白色菌落。 P.Syringae PV的反应。雷曼生产菌株是阳性的;过敏反应烟草,明胶水解,射击酶水解和阴性氧化酶反应,果胶溶液活性,精氨酸脱氢酶,酪氨酸,酒石酸。使用引物,在热循环仪中进行PCR研究,BL(5'-CTTTCGTGGTCTTGATGAGGGGAGGAGGAGGAGGAGGAGGAGGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGTC-3')。 SYRB基因752bp扩增的乳清剂。总共通过使用经典和分子鉴定试验测定41个细菌菌株,鉴定了18个菌株,鉴定了假单胞菌Syringae PV。雷丁。

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