检测凡纳滨对虾(Litopenaeus vannamei)副溶血性弧菌毒素基因的 DNA 分离方法比较

N. Lestari
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引用次数: 0

摘要

副溶血性弧菌是凡纳滨对虾(Litopenaeus vannamei)养殖中的危险病原体之一。感染这种细菌会导致对虾大量死亡,给养殖户造成巨大损失。这种细菌也有一种特殊的基因,即 toxR 基因,用于检测它的存在。能否成功检测到这种细菌,决定了能否成功处理它引起的疾病。本研究的目的是确定检测凡纳滨对虾中副溶血性弧菌毒素 R 基因的最佳 DNA 分离方法。研究采用了基于分子生物学的鉴定方法,使用了两种 DNA 分离方案,即氯仿和波林裂解缓冲液。可视化结果显示,在胰蛋白酶大豆肉汤(TSB)培养基培养制备过程中,用沸腾裂解缓冲液分离出的样本中出现了毒素R基因DNA。这说明沸腾裂解缓冲液法是检测南美白对虾副溶血性弧菌毒素R基因的一种合适的DNA分离方法。
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Komparasi Metode Isolasi DNA dalam Mendeteksi Gen toxR Bakteri Vibrio parahaemolyticus pada Udang Vaname (Litopenaeus vannamei)
Vibrio parahaemolyticus bacteria is one of the dangerous pathogens in vaname shrimp farming (Litopenaeus vannamei). Infection with this bacterium can cause mass mortality in shrimp and considerable losses for farmers. This bacterium also has a specific gene, the toxR gene, which is used to detect its presence. The successful detection of this bacterium determines the success of handling the disease it causes. The purpose of the study was to determine the optimal DNA isolation method in detecting the toxR gene of Vibrio parahaemolyticus bacteria in vaname shrimp. The research was conducted by means of molecular biology-based identification using two DNA isolation protocols, namely Chloroform and Boilling lysis buffer. Visualization results showed that toxR gene DNA appeared in samples isolated with Boiling Lysis Buffer in Tryptic Soy Broth (TSB) media culture preparation. This means that the boiling lysis buffer method is a suitable DNA isolation method for detecting the toxR gene of the Vibrio parahaemolyticus bacteria in white shrimp.
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