Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No, 189 Songling Road, Qingdao 266101, China.
Biotechnol Biofuels. 2012 Mar 21;5(1):17. doi: 10.1186/1754-6834-5-17.
Direct conversion of solar energy and carbon dioxide to drop in fuel molecules in a single biological system can be achieved from fatty acid-based biofuels such as fatty alcohols and alkanes. These molecules have similar properties to fossil fuels but can be produced by photosynthetic cyanobacteria.
Synechocystis sp. PCC6803 mutant strains containing either overexpression or deletion of the slr1609 gene, which encodes an acyl-ACP synthetase (AAS), have been constructed. The complete segregation and deletion in all mutant strains was confirmed by PCR analysis. Blocking fatty acid activation by deleting slr1609 gene in wild-type Synechocystis sp. PCC6803 led to a doubling of the amount of free fatty acids and a decrease of alkane production by up to 90 percent. Overexpression of slr1609 gene in the wild-type Synechocystis sp. PCC6803 had no effect on the production of either free fatty acids or alkanes. Overexpression or deletion of slr1609 gene in the Synechocystis sp. PCC6803 mutant strain with the capability of making fatty alcohols by genetically introducing fatty acyl-CoA reductase respectively enhanced or reduced fatty alcohol production by 60 percent.
Fatty acid activation functionalized by the slr1609 gene is metabolically crucial for biosynthesis of fatty acid derivatives in Synechocystis sp. PCC6803. It is necessary but not sufficient for efficient production of alkanes. Fatty alcohol production can be significantly improved by the overexpression of slr1609 gene.
在单一生物系统中,直接将太阳能和二氧化碳转化为燃料分子,可以通过脂肪酸基生物燃料来实现,如脂肪酸醇和烷烃。这些分子与化石燃料具有相似的性质,但可以由光合蓝藻产生。
构建了含有 slr1609 基因过表达或缺失的突变株的集胞藻 6803 突变株,slr1609 基因编码酰基辅酶 A 合成酶(AAS)。通过 PCR 分析确认了所有突变株的完全分离和缺失。在野生型集胞藻 6803 中通过删除 slr1609 基因阻断脂肪酸的激活,导致游离脂肪酸的量增加一倍,烷烃的产量减少高达 90%。在野生型集胞藻 6803 中 slr1609 基因的过表达对游离脂肪酸或烷烃的产生没有影响。在能够通过基因引入脂肪酸酰基辅酶 A 还原酶产生脂肪酸醇的集胞藻 6803 突变株中 slr1609 基因的过表达或缺失分别使脂肪酸醇的产量增加了 60%。
slr1609 基因功能化的脂肪酸激活对于集胞藻 6803 中脂肪酸衍生物的生物合成是代谢关键的。它对于烷烃的高效生产是必要的,但不是充分的。通过 slr1609 基因的过表达可以显著提高脂肪酸醇的产量。