首页> 外文期刊>Marine biotechnology >Isolation and Characterisation of a High-Efficiency Desaturase and Elongases from Microalgae for Transgenic LC-PUFA Production
【24h】

Isolation and Characterisation of a High-Efficiency Desaturase and Elongases from Microalgae for Transgenic LC-PUFA Production

机译:高效去饱和酶和微藻中转基因LC-PUFA生产的延伸酶的分离和鉴定

获取原文
获取原文并翻译 | 示例
           

摘要

The production of long-chain polyunsaturated fatty acids from precursor molecules linoleic acid (LA; 18:2 omega 6) and alpha-linolenic acid (ALA; 18:3 omega 3) is catalysed by sequential desaturase and elongase reactions. We report the isolation of a front-end Delta 6-desaturase gene from the microalgae Ostreococcus lucimarinus and two elongase genes, a Delta 6-elongase and a Delta 5-elongase, from the microalga Pyramimonas cordata. These enzymes efficiently convert their respective substrates when transformed in yeast (39-75% conversion for omega 3 substrate fatty acids), and the Delta 5-elongase in particular displays higher elongation efficiency (75% for conversion of eicosapentaenoic acid (20:5 omega 3) to docosapentaenoic acid (22:5 omega 3)) than previously reported genes. In addition, the Delta 6-desaturase is homologous with acyl-CoA desaturases and shows a strong preference for the omega 3 substrate ALA.
机译:由先驱分子亚油酸(LA; 18:2ω6)和α-亚麻酸(ALA; 18:3ω3)的长链多不饱和脂肪酸的产生是通过顺序的去饱和酶和延伸酶反应来催化的。我们报告从微藻Ostreococcus lucimarinus和两个延伸酶基因,从微藻Pyramimonas cordata的一个Delta 6-延伸酶和一个Delta 5延伸酶的前端三角洲6-去饱和酶基因的分离。当在酵母中转化时,这些酶有效地转化其各自的底物(ω3底物脂肪酸的转化率为39-75%),尤其是Delta 5-延伸酶显示出更高的延伸效率(二十碳五烯酸的转化率为75%(20:5ω) 3)比以前报道的基因多二十碳五烯酸(22:5Ω3))。另外,Delta 6-去饱和酶与酰基-CoA去饱和酶同源,并且显示出对ω3底物ALA的强烈偏好。

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