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首页> 外文期刊>Applied Microbiology and Biotechnology >Improvement of compactin (ML-236B) production by genetic engineering in compactin high-producing Penicillium citrinum
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Improvement of compactin (ML-236B) production by genetic engineering in compactin high-producing Penicillium citrinum

机译:通过基因工程改进高产紧凑型柑桔青霉菌中的紧凑型压缩机(ML-236B)生产

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An increase in compactin (ML-236B) production was achieved by introducing a whole compactin biosynthetic gene cluster or the regulatory gene mlcR into compactin high-producing Penicillium citrinum. In the previous report, we introduced mlcR encoding the positive regulator of compactin biosynthetic genes into compactin high-producing strain no. 41520, and most of the transformants produced higher amounts of compactin. Here, we characterize one of the resulting high producers (strain TIR-35, which produced 50% more compactin) and reveal that TIR-35 contained five copies of mlcR and that early, enhanced expression of mlcR caused compactin overproduction. Similarly, the introduction of mlcR into strain T48.19, which was created previously from strain no. 41520 by introducing a partial compactin biosynthetic gene cluster, enhanced compactin production further. Our results indicated that genetic engineering is an effective tool to improve compactin production, even in compactin high producers.
机译:通过将整个压紧生物素生物合成基因簇或调控基因mlcR引入压紧高产青霉素青霉素中,可以提高压紧蛋白(ML-236B)的产量。在以前的报告中,我们将编码紧密连蛋白生物合成基因的正调控子的mlcR引入了紧密连蛋白高产菌株No.。 41520,并且大多数转化子产生了更高量的紧致蛋白。在这里,我们表征了其中一个高产菌株(菌株TIR-35,其产生的致密蛋白含量提高了50%),并揭示了TIR-35含有5份mlcR拷贝,并且早期表达的mlcR增强导致致密蛋白的过度生产。同样,将mlcR引入菌株T48.19,该菌株先前是从No. 41520通过引入部分压紧蛋白生物合成基因簇,进一步提高了压紧蛋白的产量。我们的结果表明,基因工程是即使在高密度素生产者中也可以提高紧密素生产的有效工具。

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