首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Autotrophic Production of Stable-Isotope-Labeled Arginine in Ralstonia eutropha Strain H16
【2h】

Autotrophic Production of Stable-Isotope-Labeled Arginine in Ralstonia eutropha Strain H16

机译:Ralstonia eutropha富营养菌株H16中稳定同位素标记的精氨酸的自养生产。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

With the aim of improving industrial-scale production of stable-isotope (SI)-labeled arginine, we have developed a system for the heterologous production of the arginine-containing polymer cyanophycin in recombinant strains of Ralstonia eutropha under lithoautotrophic growth conditions. We constructed an expression plasmid based on the cyanophycin synthetase gene (cphA) of Synechocystis sp. strain PCC6308 under the control of the strong PcbbL promoter of the R. eutropha H16 cbbc operon (coding for autotrophic CO2 fixation). In batch cultures growing on H2 and CO2 as sole sources of energy and carbon, respectively, the cyanophycin content of cells reached 5.5% of cell dry weight (CDW). However, in the absence of selection (i.e., in antibiotic-free medium), plasmid loss led to a substantial reduction in yield. We therefore designed a novel addiction system suitable for use under lithoautotrophic conditions. Based on the hydrogenase transcription factor HoxA, this system mediated stabilized expression of cphA during lithoautotrophic cultivation without the need for antibiotics. The maximum yield of cyanophycin was 7.1% of CDW. To test the labeling efficiency of our expression system under actual production conditions, cells were grown in 10-liter-scale fermentations fed with 13CO2 and 15NH4Cl, and the 13C/15N-labeled cyanophycin was subsequently extracted by treatment with 0.1 M HCl; 2.5 to 5 g of [13C/15N]arginine was obtained per fed-batch fermentation, corresponding to isotope enrichments of 98.8% to 99.4%.
机译:为了提高工业规模生产的稳定同位素(SI)标记的精氨酸,我们开发了一种在异养自生营养条件下在富营养的Ralstonia eutropha重组菌株中异源生产含精氨酸的聚合物蓝霉素的系统。我们构建了基于蓝藻属藻蓝藻合成酶基因(cphA)的表达质粒。菌株PCC6308受富营养芽孢杆菌H16 cbbc操纵子的强PcbbL启动子控制(编码自养CO2固定)。在分别以H2和CO2作为唯一能源和碳源生长的分批培养物中,细胞的蓝霉素含量达到细胞干重(CDW)的5.5%。然而,在没有选择的情况下(即在无抗生素的培养基中),质粒的损失导致产量的大幅降低。因此,我们设计了一种新型的成瘾系统,适合在自养石条件下使用。基于加氢酶转录因子HoxA,该系统介导了石自养培养过程中cphA的稳定表达,而无需使用抗生素。蓝霉素的最大产量为CDW的7.1%。为了测试我们的表达系统在实际生产条件下的标记效率,将细胞在10公升规模的发酵中培养,发酵中加入了 13 CO2和 15 NH4Cl,随后用0.1 M HCl处理,提取> 13 C / 15 N标记的蓝霉素。每次分批补料发酵可得到2.5至5 g [ 13 C / 15 N]精氨酸,对应于98.8%至99.4%的同位素富集。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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