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首页> 外文期刊>Applied Microbiology and Biotechnology >Improving polyhydroxyalkanoate production by knocking out the genes involved in exopolysaccharide biosynthesis in Haloferax mediterranei
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Improving polyhydroxyalkanoate production by knocking out the genes involved in exopolysaccharide biosynthesis in Haloferax mediterranei

机译:通过敲除地中海嗜盐菌中胞外多糖生物合成相关基因来提高多羟基链烷酸酯的生产

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摘要

Haloferax mediterranei is capable of producing large amounts of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) from many kinds of carbon sources, with exopolysaccharide (EPS) as a by-product. In this study, we identified a gene cluster involved in EPS biosynthesis in H. mediterranei. Knocking out the genes in this cluster encoding the putative UDP-N-acetylglucosamine 6-dehydrogenase (HFX-2145), glycosyltransferases (HFX-2146 and HFX-2147) and polysaccharide transporter (HFX-2148) eliminated EPS synthesis. The deficiency in EPS biosynthesis in the mutant strain remarkably decreased the viscosity of culture broth, and hence increased the dissolved oxygen content and decreased the foaming propensity. Compared with the wild-type (WT) strain, the PHBV production of the EPS-mutant strain was significantly enhanced (approximately 20 %), whereas the cell growth rate remained similar under the same culture conditions. These results indicated that the carbon sources used for synthesizing EPS were shifted to PHBV production. Thus, a novel engineered H. mediterranei strain was developed, which would be favorable for future industrial production of PHBV.
机译:Haloferax mediterranei能够从多种碳源中产生大量的聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV),并带有外多糖(EPS)作为副产物。在这项研究中,我们确定了一个基因簇,该基因簇与地中海嗜血杆菌中的EPS生物合成有关。在该簇中敲除编码推定的UDP-N-乙酰氨基葡糖6-脱氢酶(HFX-2145),糖基转移酶(HFX-2146和HFX-2147)和多糖转运蛋白(HFX-2148)的基因消除了EPS合成。突变菌株中EPS生物合成的不足显着降低了培养液的粘度,因此增加了溶解氧含量并降低了发泡倾向。与野生型(WT)菌株相比,EPS突变菌株的PHBV产量显着提高(约20%),而在相同培养条件下细胞生长速率保持相似。这些结果表明,用于合成EPS的碳源已转向PHBV生产。因此,开发了一种新的工程改造的嗜中性链球菌菌株,这将有利于PHBV的未来工业生产。

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