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Genes encoding cytochrome P450 and monooxygenase enzymes define one end of the aflatoxin pathway gene cluster in Aspergillus parasiticus

机译:编码细胞色素P450和单加氧酶的基因定义了寄生曲霉中黄曲霉毒素途径基因簇的一端

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The identification of overlapping cosmids resulted in the discovery of the aflatoxin biosynthetic pathway gene cluster in Aspergillus flavus and A. parasiticus. This finding led to the cloning and characterization of one regulatory and 16 structural genes involved in aflatoxin biosynthesis, including the most recent report on the gene, ordA, which has been identified to be involved in the formation of four aflatoxins (B-1, B-2, G(1) and G(2)). However, these genes do not account for all the identified chemical/biochemical steps in aflatoxin synthesis and efforts are underway to identify the genes controlling the other steps. We are also attempting to define the outer boundaries of the aflatoxin pathway gene cluster in the Aspergillus genome. For this goal, we extended sequencing in both directions from the existing (60 kb) aflatoxin pathway gene cluster, beyond the pksA gene at one end and the omtA gene at the other. Within the 25-kb genomic DNA sequence determined at the omtA end of the cluster, several new gene sequences were identified. The recently reported genes, vbs and ordA, were found within this 25-kb region. Two additional genes were also found in this region, a cytochrome P450 monooxygenase encoding gene, tentatively named cypX, and a monooxygenase encoding gene, tentatively named moxY, and these are also reported in this study. The sequence beyond these genes showed a 5-kb noncoding region of DNA followed by the presence of a cluster of genes probably involved in sugar metabolism. Northern blot analysis and reverse transcriptase-polymerase chain reaction (RT-PCR) studies demonstrated that the genes, cypX and MoxY are expressed concurrently with genes involved in aflatoxin biosynthesis. Therefore, the two putative aflatoxin pathway genes cypX and mox Y followed by a 5-kb non-coding region of DNA define one end of the boundary of the aflatoxin pathway gene cluster in A, parasiticus. [References: 34]
机译:重叠粘粒的鉴定导致黄曲霉和寄生曲霉中黄曲霉毒素生物合成途径基因簇的发现。这一发现导致克隆和鉴定了一个涉及黄曲霉毒素生物合成的调控基因和16个结构基因,包括关于该基因的最新报道ordA,该基因已被确定参与了四种黄曲霉毒素的形成(B-1,B -2,G(1)和G(2))。然而,这些基因不能解释黄曲霉毒素合成中所有已确定的化学/生化步骤,并且正在努力识别控制其他步骤的基因。我们还试图在曲霉基因组中定义黄曲霉毒素途径基因簇的外边界。为了实现这一目标,我们从现有(60 kb)黄曲霉毒素途径基因簇向两个方向扩展了测序,超出了一端的pksA基因和另一端的omtA基因。在簇的omtA末端确定的25-kb基因组DNA序列中,鉴定了几个新的基因序列。在这个25kb的区域内发现了最近报道的基因vbs和ordA。在该区域还发现了另外两个基因,一个细胞色素P450单加氧酶编码基因,暂定名为cypX,一个单加氧酶编码基因,暂定名为moxY,这些也在本研究中报道。这些基因以外的序列显示了一个5kb的DNA非编码区,随后出现了可能参与糖代谢的一系列基因。 Northern印迹分析和逆转录聚合酶链反应(RT-PCR)研究表明,cypX和MoxY基因与黄曲霉毒素生物合成相关基因同时表达。因此,两个假定的黄曲霉毒素途径基因cypX和mox Y,随后是DNA的5kb非编码区,定义了寄生虫A中黄曲霉毒素途径基因簇的边界的一端。 [参考:34]

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