Display options
Share it on

Biotechnol Biofuels. 2012 Mar 21;5(1):17. doi: 10.1186/1754-6834-5-17.

Effects of fatty acid activation on photosynthetic production of fatty acid-based biofuels in Synechocystis sp. PCC6803.

Biotechnology for biofuels

Qianqian Gao, Weihua Wang, Hui Zhao, Xuefeng Lu

Affiliations

  1. Key Laboratory of Biofuels, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, No, 189 Songling Road, Qingdao 266101, China. [email protected].

PMID: 22433663 PMCID: PMC3366867 DOI: 10.1186/1754-6834-5-17

Abstract

BACKGROUND: 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.

RESULTS: 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.

CONCLUSIONS: 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.

References

  1. Metab Eng. 2010 Jan;12(1):70-9 - PubMed
  2. Can J Biochem Physiol. 1959 Aug;37(8):911-7 - PubMed
  3. J Biol Chem. 1992 Jun 15;267(17):11806-10 - PubMed
  4. Methods Enzymol. 1988;167:703-12 - PubMed
  5. Microbiology (Reading). 2007 Apr;153(Pt 4):1261-1267 - PubMed
  6. Science. 2010 Jul 30;329(5991):559-62 - PubMed
  7. Plant Physiol. 2010 Mar;152(3):1598-610 - PubMed
  8. J Ind Microbiol Biotechnol. 2009 Apr;36(4):471-9 - PubMed
  9. Nat Biotechnol. 2008 Mar;26(3):298-9 - PubMed
  10. J Am Chem Soc. 2011 Mar 16;133(10):3316-9 - PubMed
  11. Plant Physiol. 2000 Mar;122(3):635-44 - PubMed
  12. J Biol Chem. 1987 Apr 15;262(11):5159-69 - PubMed
  13. J Biol Chem. 1982 Sep 25;257(18):10759-65 - PubMed
  14. Chembiochem. 2009 Jul 20;10(11):1869-77 - PubMed
  15. J Gen Microbiol. 1974 Aug;83(2):399-405 - PubMed
  16. Nat Biotechnol. 2009 Dec;27(12):1177-80 - PubMed
  17. Metab Eng. 2011 Mar;13(2):169-76 - PubMed

Publication Types