Manipulating fatty acid biosynthesis in microalgae for biofuel through protein-protein interactions

PLoS One. 2012;7(9):e42949. doi: 10.1371/journal.pone.0042949. Epub 2012 Sep 13.

Abstract

Microalgae are a promising feedstock for renewable fuels, and algal metabolic engineering can lead to crop improvement, thus accelerating the development of commercially viable biodiesel production from algae biomass. We demonstrate that protein-protein interactions between the fatty acid acyl carrier protein (ACP) and thioesterase (TE) govern fatty acid hydrolysis within the algal chloroplast. Using green microalga Chlamydomonas reinhardtii (Cr) as a model, a structural simulation of docking CrACP to CrTE identifies a protein-protein recognition surface between the two domains. A virtual screen reveals plant TEs with similar in silico binding to CrACP. Employing an activity-based crosslinking probe designed to selectively trap transient protein-protein interactions between the TE and ACP, we demonstrate in vitro that CrTE must functionally interact with CrACP to release fatty acids, while TEs of vascular plants show no mechanistic crosslinking to CrACP. This is recapitulated in vivo, where overproduction of the endogenous CrTE increased levels of short-chain fatty acids and engineering plant TEs into the C. reinhardtii chloroplast did not alter the fatty acid profile. These findings highlight the critical role of protein-protein interactions in manipulating fatty acid biosynthesis for algae biofuel engineering as illuminated by activity-based probes.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acyl Carrier Protein / chemistry
  • Acyl Carrier Protein / metabolism
  • Amino Acid Sequence
  • Biofuels*
  • Chlamydomonas reinhardtii / genetics
  • Chlamydomonas reinhardtii / metabolism
  • Chloroplasts / metabolism
  • Fatty Acids / biosynthesis*
  • Gene Expression
  • Microalgae / genetics
  • Microalgae / metabolism*
  • Molecular Docking Simulation
  • Molecular Sequence Data
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • Protein Binding
  • Protein Conformation
  • Proteins / metabolism*
  • Sequence Alignment
  • Substrate Specificity
  • Thiolester Hydrolases / chemistry
  • Thiolester Hydrolases / metabolism

Substances

  • Acyl Carrier Protein
  • Biofuels
  • Fatty Acids
  • Plant Proteins
  • Proteins
  • Thiolester Hydrolases

Grants and funding

Funding was provided by the United States Department of Energy (DOE) DE-EE0003373; United States National Science Foundation (NSF) 0742551; Rubicon Postdoctoral Fellowship; and California Energy Commission CILMSF 500-10-039. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.