Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6491053 | Journal of Biotechnology | 2015 | 10 Pages |
Abstract
Linoleate 13-hydratase from Lactobacillus acidophilus LMG 11470 converted linoleic acid to hydroxyl fatty acid, which was identified as 13S-hydroxy-9(Z)-octadecenoic acid (13-HOD) by GC-MS and NMR. The expression of linoleate 13-hydratase gene in Escherichia coli was maximized by using pACYC plasmid and super optimal broth with catabolite repression (SOC) medium containing 40 mM Mg2+. To optimize induction conditions, recombinant cells were cultivated at 37 °C, 1 mM isopropyl-β-d-thiogalactopyranoside was added at 2 h, and the culture was further incubated at 16 °C for 18 h. Recombinant cells expressing linoleate 13-hydratase from L. acidophilus were obtained under the optimized expression conditions and used for 13-HOD production from linoleic acid. The optimal reaction conditions were pH 6.0, 40 °C, 0.25% (v/v) Tween 40, 25 g lâ1 cells, and 100 g lâ1 linoleic acid, and under these conditions, whole recombinant cells produced 79 g lâ1 13-HOD for 3 h with a conversion yield of 79% (w/w), a volumetric productivity of 26.3 g lâ1 hâ1, and a specific productivity of 1.05 g g-cellsâ1 hâ1. To the best of our knowledge, the recombinant cells produced hydroxy fatty acid with the highest concentration and productivity reported so far.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Ji-Young Park, Seon-Hwa Lee, Kyoung-Rok Kim, Jin-Byung Park, Deok-Kun Oh,