| Literature DB >> 26015260 |
Ji-Young Park1, Seon-Hwa Lee1, Kyoung-Rok Kim1, Jin-Byung Park2, Deok-Kun Oh3.
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 40mM Mg(2+). To optimize induction conditions, recombinant cells were cultivated at 37°C, 1mM isopropyl-β-d-thiogalactopyranoside was added at 2h, and the culture was further incubated at 16°C for 18h. 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, 25gl(-1) cells, and 100gl(-1) linoleic acid, and under these conditions, whole recombinant cells produced 79gl(-1) 13-HOD for 3h with a conversion yield of 79% (w/w), a volumetric productivity of 26.3gl(-1)h(-1), and a specific productivity of 1.05g g-cells(-1)h(-1). To the best of our knowledge, the recombinant cells produced hydroxy fatty acid with the highest concentration and productivity reported so far. CrownEntities:
Keywords: 13S-Hydroxy-9(Z)-octadecenoic acid; Lactobacillus acidophilus; Linoleate 13-hydratase; Linoleic acid; Whole cell conversion
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Year: 2015 PMID: 26015260 DOI: 10.1016/j.jbiotec.2015.05.006
Source DB: PubMed Journal: J Biotechnol ISSN: 0168-1656 Impact factor: 3.307