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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and sequence analysis of a PVGOX gene encoding glucose oxidase in Penicillium viticola Fl strain and it's expression quantitation
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Molecular cloning and sequence analysis of a PVGOX gene encoding glucose oxidase in Penicillium viticola Fl strain and it's expression quantitation

机译:葡萄青霉Fl菌株中编码葡萄糖氧化酶的PVGOX基因的分子克隆,序列分析及表达定量

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摘要

The PVGOX gene (accession number: KT452630) was isolated from genomic DNA of the marine fungi Penicillium viticola Fl by Genome Walking and their expression analysis was done by Fluorescent RT-PCR. An open reading frame of 1806 bp encoding a 601 amino acid protein (isoelectric point: 5.01) with a calculated molecular weight of 65,535.4 was characterized. The deduced protein showed 75%, 71%, 69% and 64% identity to those deduced from the glucose oxidase (GOX) genes from different fungal strains including; Talaromyces variabilis, Beauveria bassiana, Aspergillus terreus, and Aspergillus niger, respectively. The promoter of the gene (intronless) had two TATA boxes around the base pair number 88 and 94 and as well as a CAAT box at 100. However, the terminator of the PVGOX gene does not contain any polyadenylation site (AATAAA). The protein deduced from the PVGOX gene had a signal peptide containing 17 amino acids, three cysteine residues and six potential N-linked glycosylation sites, among them, -N-K-T-Y- at 41 amino acid, -N-R-S-L- at 113 amino acid, -N-G-T-I- at 192 amino acid, -N-T-T-A at 215 amino acid, -N-F-T-E at 373 amino acid and -N-V-T-A- at 408 amino acid were the most possible N-glycosylation sites. Furthermore, the relative transcription level of the PVGOX gene was also stimulated in the presence of 4% (w/v) of calcium carbonate and 0.5 % (v/v) of CSL in the production medium compared with that of the PVGOX gene when the fungal strain Fl was grown in the absence of calcium carbonate and CSL in the production medium, suggesting that under the optimal conditions, the expression of the PVGOX gene responsible for gluconic acid biosynthesis was enhanced, leading to increased gluconic acid production. Therefore, the highly glycosylated oxidase enzyme produced by P. viticola Fl strain might be a good producer in the fermentation process for the industrial level production of gluconic acid. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过基因组步行从海洋真菌葡萄小青霉F1的基因组DNA中分离出PVGOX基因(登录号:KT452630),并通过荧光RT-PCR进行了表达分析。表征了一个1806 bp的开放阅读框,该框编码了一个601氨基酸蛋白(等电点:5.01),计算分子量为65535.4。推导的蛋白质与从不同真菌菌株的葡萄糖氧化酶(GOX)基因推导的蛋白质具有75%,71%,69%和64%的同一性。可变孢菌(Talaromyces variabilis),球孢白僵菌(Berveria bassiana),土曲霉(Aspergillus terreus)和黑曲霉(Aspergillus niger)。该基因的启动子(无内含子)在碱基对编号88和94处有两个TATA框,在100个碱基对处有一个CAAT框。但是,PVGOX基因的终止子不包含任何聚腺苷酸化位点(AATAAA)。从PVGOX基因推导的蛋白质的信号肽包含17个氨基酸,3个半胱氨酸残基和6个潜在的N-连接糖基化位点,其中-41位氨基酸为-NKTY-,113位氨基酸为-NRSL-,-NGTI-最可能的N-糖基化位点是在192个氨基酸处,在215个氨基酸处的-NTTA,在373个氨基酸处的-NFTE和在408个氨基酸处的-NVTA-。此外,与PVGOX基因相比,当生产培养基中存在4%(w / v)的碳酸钙和0.5%(v / v)的CSL时,也会刺激PVGOX基因的相对转录水平。真菌菌株F1在生产培养基中不存在碳酸钙和CSL的情况下生长,这表明在最佳条件下,负责葡萄糖酸生物合成的PVGOX基因的表达增强,导致葡萄糖酸产量增加。因此,由葡萄球菌F1菌株产生的高度糖基化的氧化酶可能是用于工业水平生产葡萄糖酸的发酵过程中的良好生产者。 (C)2016 Elsevier B.V.保留所有权利。

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