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Phosphorylation of Nucleosides by the Mutated Acid Phosphatase from Morganella morganii

机译:摩根氏摩根氏菌中突变的酸性磷酸酶将核苷磷酸化

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A novel nucleoside phosphorylation process using the food additive pyrophosphate as the phosphate source was investigated. TheMorganella morganii gene encoding a selective nucleoside pyrophosphate phosphotransferase was cloned. It was identical to theM. morganii PhoC acid phosphatase gene. Sequential in vitro random mutagenesis was performed on the gene by error-prone PCR to construct a mutant library. The mutant library was introduced intoEscherichia coli, and the transformants were screened for the production of 5′-IMP. One mutated acid phosphatase with an increased phosphotransferase reaction yield was obtained. With E. coli overproducing the mutated acid phosphatase, 101 g of 5′-IMP per liter (192 mM) was synthesized from inosine in an 88% molar yield. This improvement was achieved with two mutations, Gly to Asp at position 92 and Ile to Thr at position 171. A decreasedKm value for inosine was responsible for the increased productivity.
机译:研究了一种以食品添加剂焦磷酸盐为磷酸盐源的新型核苷磷酸化方法。克隆了编码选择性核苷焦磷酸磷酸转移酶的 Morganella morganii 基因。它与 M相同。 PhoC酸磷酸酶基因。通过易错PCR对该基因进行顺序的体外随机诱变,以构建突变体文库。将突变体文库导入大肠杆菌,并筛选转化子以产生5'-IMP。获得一种具有增加的磷酸转移酶反应产率的突变的酸性磷酸酶。使用 E。过量生产突变型酸性磷酸酶的大肠杆菌,从肌苷以每摩尔88%的摩尔比合成了101 g 5'-IMP /升(192 mM)。这种改善是通过两个突变实现的,第92位的Gly突变为Asp,第171位的Ile突变为Thr。肌苷的 K m 值降低是生产力提高的原因。

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