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Heterologous Production of a Novel Cyclic Peptide Compound, KK-1, in Aspergillus oryzae

机译:米曲霉中异源生产新型环状肽化合物KK-1

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A novel cyclic peptide compound, KK-1, was originally isolated from the plant-pathogenic fungus Curvularia clavata . It consists of 10 amino acid residues, including five N -methylated amino acid residues, and has potent antifungal activity. Recently, the genome-sequencing analysis of C. clavata was completed, and the biosynthetic genes involved in KK-1 production were predicted by using a novel gene cluster mining tool, MIDDAS-M. These genes form an approximately 75-kb cluster, which includes nine open reading frames, containing a non-ribosomal peptide synthetase (NRPS) gene. To determine whether the predicted genes were responsible for the biosynthesis of KK-1, we performed heterologous production of KK-1 in Aspergillus oryzae by introduction of the cluster genes into the genome of A. oryzae . The NRPS gene was split in two fragments and then reconstructed in the A. oryzae genome, because the gene was quite large (approximately 40 kb). The remaining seven genes in the cluster, excluding the regulatory gene kkR , were simultaneously introduced into the strain of A. oryzae in which NRPS had already been incorporated. To evaluate the heterologous production of KK-1 in A. oryzae , gene expression was analyzed by RT-PCR and KK-1 productivity was quantified by HPLC. KK-1 was produced in variable quantities by a number of transformed strains, along with expression of the cluster genes. The amount of KK-1 produced by the strain with the greatest expression of all genes was lower than that produced by the original producer, C. clavata . Therefore, expression of the cluster genes is necessary and sufficient for the heterologous production of KK-1 in A. oryzae , although there may be unknown factors limiting productivity in this species.
机译:最初从植物病原真菌Curvularia clavata中分离出一种新型的环肽化合物KK-1。它由10个氨基酸残基组成,其中包括5个N-甲基化氨基酸残基,并且具有有效的抗真菌活性。最近,完成了对C. clavata的基因组测序分析,并使用新型基因簇挖掘工具MIDDAS-M预测了参与KK-1生产的生物合成基因。这些基因形成大约75 kb的簇,其中包括9个开放阅读框,其中包含一个非核糖体肽合成酶(NRPS)基因。为了确定预测的基因是否负责KK-1的生物合成,我们通过将簇基因导入米曲霉的基因组中,在米曲霉中进行了KK-1的异源生产。 NRPS基因被分为两个片段,然后在米曲霉基因组中重建,因为该基因非常大(约40 kb)。除调节基因kkR外,簇中其余的七个基因同时被引入已掺入NRPS的米曲霉菌株中。为了评估米曲霉中KK-1的异源产生,通过RT-PCR分析基因表达,并通过HPLC定量KK-1生产力。 KK-1由许多转化菌株以及簇基因的表达以可变数量产生。在所有基因中表达最高的菌株所产生的KK-1量要低于原始生产者C. clavata所产生的量。因此,簇基因的表达对于米曲霉中KK-1的异源产生是必要的和充分的,尽管可能存在未知的因素限制了该物种的生产力。

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