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戊酮糖二酸单胞菌的基因工程改造以提高 2-酮基-L-古洛糖酸的产量。

Genetic engineering of Ketogulonigenium vulgare for enhanced production of 2-keto-L-gulonic acid.

机构信息

Dept Biological Sciences and Biotechnology, MOE Key Lab. Bioinformatics (& System Biology), Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

出版信息

J Biotechnol. 2012 Jan 20;157(2):320-5. doi: 10.1016/j.jbiotec.2011.12.004. Epub 2011 Dec 14.

Abstract

Folate derivatives are crucial growth factors for Ketogulonigenium vulgare which is used in mixed culture with Bacillus megaterium for the industrial production of 2-keto-L-gulonic acid (2-KGA), the precursor of L-ascorbic acid (L-AA) or vitamin C (Vc). To improve the growth and 2-KGA production, five genes involved in folate biosynthesis identified in a folate gene cluster from Lactococcus lactis MG1363, including folB, folKE, folP, folQ and folC, were over-expressed in K. vulgare. Intracellular folate concentration in the recombinant strain harboring folate biosynthesis genes cluster under the control of P(sdh) (sorbose dehydrogenase gene sdh promoter from K. vulgare) was 8 times higher than that of the wildtype K. vulgare DSM 4025 (P<0.001). In shake flask studies, the cell density and 2-KGA production of the recombinant K. vulgare Rif (pMCS2PsdhfolBC) were increased by 18% (P<0.001) and 14% (P<0.001), respectively, under a relatively stable pH 7 condition. In fermentor studies, enhancements around 25% cell density (P<0.001) and approximately 35% 2-KGA productivity (P<0.001) were observed in comparison with the controls without over-expressing the folate biosynthesis genes. This was the first successful study of metabolic engineering on K. vulgare for enhanced 2-KGA production.

摘要

叶酸衍生物是酮古龙酸菌(Ketogulonigenium vulgare)的重要生长因子,该菌与巨大芽孢杆菌混合培养,用于工业生产 2-酮-L-古龙酸(2-KGA),这是 L-抗坏血酸(L-AA)或维生素 C(Vc)的前体。为了提高生长和 2-KGA 产量,在乳球菌 MG1363 的叶酸基因簇中鉴定出 5 个与叶酸生物合成有关的基因,包括 folB、folKE、folP、folQ 和 folC,在酮古龙酸菌中过表达。在重组菌中,在 P(sdh)(来自酮古龙酸菌的 sorbose 脱氢酶基因 sdh 启动子)控制下,叶酸生物合成基因簇的细胞内叶酸浓度比野生型酮古龙酸菌 DSM 4025 高 8 倍(P<0.001)。在摇瓶研究中,在相对稳定的 pH7 条件下,重组酮古龙酸菌 Rif(pMCS2PsdhfolBC)的细胞密度和 2-KGA 产量分别提高了 18%(P<0.001)和 14%(P<0.001)。在发酵罐研究中,与未过表达叶酸生物合成基因的对照相比,细胞密度提高了约 25%(P<0.001),2-KGA 生产力提高了约 35%(P<0.001)。这是首次成功地对酮古龙酸菌进行代谢工程改造以提高 2-KGA 产量的研究。

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