Artificial covalent linkage of bacterial acyl carrier proteins for fatty acid production

March 24, 2020

Title

Artificial covalent linkage of bacterial acyl carrier proteins for fatty acid production

Author

Carlos Rullán-Lind, Melissa Ortiz-Rosario, Andrea García-González, Vivian Stojanoff, Nataliya E. Chorna, Ruth B. Pietri, Abel Baerga-Ortiz

Year

2019

Journal

Scientific Reports

Abstract

Acyl carrier proteins (ACPs) are essential to the production of fatty acids. In some species of marine bacteria, ACPs are arranged into tandem repeats joined by peptide linkers, an arrangement that results in high fatty acid yields. By contrast, Escherichia coli, a relatively low producer of fatty acids, uses a single-domain ACP. In this work, we have engineered the native E. coli ACP into tandem di- and tri-domain constructs joined by a naturally occurring peptide linker from the PUFA synthase of Photobacterium profundum. The size of these tandem fused ACPs was determined by size exclusion chromatography to be higher (21 kDa, 36 kDa and 141 kDa) than expected based on the amino acid sequence (12 kDa, 24 kDa and 37 kDa, respectively) suggesting the formation of a flexible extended conformation. Structural studies using small-angle X-ray scattering (SAXS), confirmed this conformational flexibility. The thermal stability for the di- and tri-domain constructs was similar to that of the unfused ACP, indicating a lack of interaction between domains. Lastly, E. coli cultures harboring tandem ACPs produced up to 1.6 times more fatty acids than wild-type ACP, demonstrating the viability of ACP fusion as a method to enhance fatty acid yield in bacteria.

Instrument

J-1500

Keywords

Circular dichroism, Thermal stability, Protein folding, Secondary structure, Biochemistry