首页> 外文期刊>Journal of Agricultural and Food Chemistry >Lower Citrinin Production by Gene Disruption of ctnB Involved in Citrinin Biosynthesis in Monascus aurantiacus Li AS3.4384
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Lower Citrinin Production by Gene Disruption of ctnB Involved in Citrinin Biosynthesis in Monascus aurantiacus Li AS3.4384

机译:通过破坏ctnB基因参与产黄曲霉李AS3.4384的Citrinin生物合成来降低Citrinin的产生

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The filamentous fungi Monascus spp. have been used in the production of food colorants and health remedies for more than 1000 years in Asia. However, greater attention has been given to the safety of Monascus products because they contain citrinin, which is harmful to the hepatic and renal systems. The citrinin biosynthetic gene cluster has been characterized in Monasucs aurantiacus. The ctnB gene encoding an oxidoreductase is located between pksCT and ctnA. In this study, a ctnB replacement vector (pCTNB-HPH) was constructed to disrupt the ctnB gene with a hygromycin resistance gene as the selection marker. The linear vector was transformed into M. aurantiacus using the protoplast CaCl2/polyethylene glycol (PEG) method. Three ctnB-disrupted strains were obtained by homologous recombination. In comparison to the parental strain, the ActnB mutants barely produced citrinin. These data confirmed that the ctnB gene is directly involved in citrinin biosynthesis. Moreover, the yields of the pigments of two disruptants were similar to that of the wild-type strain, but the yield of another mutant was slightly higher than that of the latter strain. These results indicate that the production of the mycotoxin citrinin was successfully eliminated through genetic engineering.
机译:丝状真菌红曲菌属。在亚洲,已经有超过1000年的历史将其用于生产食品着色剂和保健药物。但是,红曲霉产品的安全性得到了更多的关注,因为它们含有对肝脏和肾脏系统有害的西林蛋白。桔黄素生物合成基因簇已在红曲霉中表征。编码氧化还原酶的ctnB基因位于pksCT和ctnA之间。在这项研究中,构建了一个ctnB替代载体(pCTNB-HPH),以潮霉素抗性基因作为选择标记来破坏ctnB基因。使用原生质体CaCl2 /聚乙二醇(PEG)方法将线性载体转化为金黄色葡萄球菌。通过同源重组获得了三个破坏ctnB的菌株。与亲本菌株相比,ActnB突变体几乎不产生citrinin。这些数据证实了ctn​​B基因直接参与了橘皮素的生物合成。此外,两种破坏剂的色素产量与野生型菌株相似,但另一突变体的产量略高于后者。这些结果表明通过基因工程成功地消除了霉菌毒素柠檬素的产生。

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