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首页> 外文期刊>International microbiology: the official journal of the Spanish Society for Microbiology >Penicillin G acylase production by Mucor griseocyanus and the partial genetic analysis of its pga gene
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Penicillin G acylase production by Mucor griseocyanus and the partial genetic analysis of its pga gene

机译:青霉素G酰化酶产生的粘膜Griseocyanus和其PGA基因的部分遗传分析

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Penicillin acylases (penicillin amidohydrolase, EC 3.5.1.11) are a group of enzymes with many applications within the pharmaceutical industry, and one of them is the production of semi-synthetic beta-lactam antibiotics. This enzyme is mainly produced by bacteria but also by some fungi. In the present study, the filamentous fungus Mucor griseocyanus was used to produce penicillin acylase enzyme (PGA). Its ability to express PGA enzyme in submerged fermentation process was assessed, finding that this fungal strain produces the biocatalyst of interest in an extracellular way at a level of 570?IU/L at 72?h of fermentation; in this case, a saline media using lactose as carbon source and penicillin G as inducer was employed. In addition, a DNA fragment (859?bp) of the pga from a pure Mucor griseocyanus strain was amplified, sequenced, and analyzed in silico. The partial sequence of pga identified in the fungi showed high identity percentage with penicillin G acylase sequences deposited in NCBI through BLAST, especially with the β subunit of PGA from the Alcaligenes faecalis bacterium? which is a region involved in the catalytic function of this protein. Besides, the identification of domains in the penicillin G acylase sequence of Mucor griseocyanus showed three conserved regions of this protein. The bioinformatic results support the identity of the gen as penicillin G acylase. This is the first report that involves sequencing and in silico analysis of Mucor griseocyanus strain gene encoding PGA.
机译:青霉素酰基酶(青霉素amidoHoldolase,EC 3.5.1.11)是一组具有许多在制药工业中的应用,其中一个是半合成β-内酰胺抗生素的生产。该酶主要由细菌产生,但也由一些真菌产生。在本研究中,丝状真菌粘膜霉菌术用于生产青霉素酰化酶(PGA)。评估其表达PGA酶在浸没式发酵过程中的能力,发现该真菌菌株以细胞外的方式在570℃的细胞外的方式产生生物催化剂,在570?IU / L处于发酵的情况下;在这种情况下,采用使用乳糖作为碳源和青霉素G作为诱导剂的盐培养基。另外,从纯粘膜晶胞菌株中的PGA的DNA片段(859〜BP)扩增,测序和分析并在硅中分析。真菌中鉴定的PGA的部分序列显示通过爆炸在NCBI沉积的青霉素G酰化酶序列的高同型百分比,特别是来自阿尔卡里酮群细菌的PGA的β亚基?这是参与该蛋白质催化功能的区域。此外,粘膜Griseocyanus的青霉素G酰基酶序列中的域鉴定为该蛋白质的三个保守区域。生物信息结果支持作为青霉素G酰化酶的原因的同一性。这是第一个涉及测序和编码PGA的粘膜Griseocyanus菌株基因的硅分析的第一个报告。

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