...
首页> 外文期刊>Applied and Environmental Microbiology >Production of poly(3-hydroxybutyrate) by fed-batch culture of filamentation-suppressed recombinant Escherichia coli.
【24h】

Production of poly(3-hydroxybutyrate) by fed-batch culture of filamentation-suppressed recombinant Escherichia coli.

机译:通过补料分批培养丝状抑制的重组大肠杆菌生产聚(3-羟基丁酸酯)。

获取原文

摘要

Recombinant Escherichia coli XL1-Blue harboring a high-copy-number plasmid containing the Alcaligenes eutrophus polyhydroxyalkanoate synthesis genes could efficiently synthesize poly(3-hydroxybutyrate) (PHB) in a complex medium containing yeast extract and tryptone but not in a defined medium. One of the reasons for the reduced PHB production in a defined medium was thought to be severe filamentation of cells in this medium. By overexpressing an essential cell division protein, FtsZ, in recombinant E. coli producing PHB, filamentation could be suppressed and PHB could be efficiently produced in a defined medium. A high PHB concentration of 149 g/liter, with high productivity of 3.4 g of PHB/liter/h, could be obtained by the pH-stat fed-batch culture of the filamentation-suppressed recombinant E. coli in a defined medium. It was also found that insufficient oxygen supply at a dissolved oxygen concentration (DOC) of 1 to 3% of air saturation during active PHB synthesis phase did not negatively affect PHB production. By growing cells to the concentration of 110 g/liter and then controlling the DOC in the range of 1 to 3% of air saturation, a PHB concentration of 157 g/liter and PHB productivity of 3.2 g of PHB/liter/h were obtained. For the scale-up studies, fed-batch culture was carried out in a 50-liter stirred tank fermentor, in which the DOC decreased to zero when cell concentration reached 50 g/liter. However, a relatively high PHB concentration of 101 g/liter and PHB productivity of 2.8 g of PHB/liter/h could still be obtained, which demonstrated the possibility of industrial production of PHB in a defined medium by employing the filamentation-suppressed recombinant E. coli.
机译:带有高拷贝数质粒的重组大肠杆菌XL1-Blue包含含有真核嗜碱菌的多羟基链烷酸酯合成基因,可以在含有酵母提取物和胰蛋白complex的复杂培养基中有效合成聚(3-羟基丁酸)(PHB),但不能在确定的培养基中合成。在确定的培养基中减少PHB产生的原因之一被认为是该培养基中细胞的严重丝化。通过在生产大肠杆菌的PHB中过量表达必需的细胞分裂蛋白FtsZ,可以抑制丝状化,并可以在限定的培养基中有效生产PHB。通过在确定的培养基中抑制丝状化的重组大肠杆菌的pH静态补料分批培养,可以获得149 g /升的高PHB浓度和3.4 g PHB /升/ h的高生产率。还发现在活性PHB合成阶段,溶解氧浓度(DOC)为空气饱和度的1-3%时,氧气供应不足,不会对PHB产生负面影响。通过将细胞生长至110 g / l的浓度,然后将DOC控制在空气饱和度的1-3%范围内,可以得到157 g / l的PHB浓度和3.2 g PHB / l / h的PHB生产率。 。为了进行放大研究,在50升搅拌罐发酵罐中进行分批补料培养,其中当细胞浓度达到50克/升时,DOC降至零。但是,仍然可以获得相对较高的PHB浓度101 g / l和PHB生产率2.8 g PHB / l / h,这表明通过使用抑制丝化的重组E可以在特定培养基中工业生产PHB。大肠杆菌

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号