首页> 外文期刊>Journal of industrial microbiology & biotechnology >Cloning and knockout of phytoene desaturase gene in Sphingomonas elodea ATCC 31461 for economic recovery of gellan gum
【24h】

Cloning and knockout of phytoene desaturase gene in Sphingomonas elodea ATCC 31461 for economic recovery of gellan gum

机译:鞘氨醇单胞菌ATCC 31461植保体去饱和酶基因的克隆和敲除,以经济回收结冷胶

获取原文
获取原文并翻译 | 示例
           

摘要

A gene encoding phytoene desaturase (crtI) in the carotenoid biosynthetic pathway of Sphingomonas elodea ATCC 31461, an industrial gellan gum-producing strain, was cloned and identified. This gene is predicted to encode a 492-amino acid protein with significant homology to the phytoene desaturase of other carotenogenic organisms. Knockout of crtI gene blocked yellow carotenoid pigment synthesis and resulted in the accumulation of colorless phytoene, confirming that it encodes phytoene desaturase. Further research indicates that the yield of gellan gum production by crtI gene knockout mutants is almost the same as that by the wild-type strain. In addition, a recovery method based on the colorless fermentation broth of the crtI gene knockout mutant was investigated. Compared to the volume of alcohol for the parent strain, much less alcohol (30%) is required in this recovery process; thus, the costs of downstream purification of gellan gum can be substantially reduced.
机译:克隆并鉴定了鞘氨醇单胞菌ATCC 31461(一种产结冷胶的产菌株)的类胡萝卜素生物合成途径中编码八氢番茄红素去饱和酶(crtI)的基因。预计该基因编码与其他致龋生物的八氢番茄红素去饱和酶具有显着同源性的492个氨基酸。 crtI基因的敲除阻止了黄色类胡萝卜素的合成,并导致了无色的八氢番茄红素的积累,证实了它编码八氢番茄红素去饱和酶。进一步的研究表明,crtI基因敲除突变体的结冷胶产量与野生株几乎相同。另外,研究了基于crtI基因敲除突变体的无色发酵液的回收方法。与亲本菌株的酒精量相比,此回收过程所需的酒精量少得多(30%);因此,可以显着降低结冷胶下游纯化的成本。

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