Extractive Fermentation of Lactic Acid with Hiochi Bacteria in a Two-Liquid Phase SystemMichiaki Matsumoto*, Masashi Nishimura, Hiroaki Kobayashi and Kazuo Kondo
Department of Chemical Engineering and Materials Science, Doshisha University, Kyotanabe, Japan
- *Corresponding Author:
- Michiaki Matsumoto
Department of Chemical Engineering and Materials Science
E-mail: [email protected]
Received date: March 17, 2016; Accepted date: April 25, 2016; Published date: May 05, 2016
Citation: Matsumoto M, Nishimura M, Kobayashi H, Kazuo K (2016) Extractive Fermentation of Lactic Acid with Hiochi Bacteria in a Two-Liquid Phase System. Ferment Technol 5:129. doi:10.4172/2167-7972.1000129
Copyright: © 2016 Matsumoto M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Lactic acid production by fermentation has attracted interest because optically pure lactic acid is the raw material of biodegradable polymer, polylactic acid, which has been mainly used in food packing. In situ extractive fermentation of lactic acid with reactive extraction has two critical problems: the toxicity of diluents and extractant and the difference in the optimum pH between fermentation and reactive extraction. In this study, the extractive fermentation was conducted with alcohol-tolerant Hiochi bacteria, Lactobacillus homohiochii and Lactobacillus fructivorans, using the co-encapsulation of the bacteria and calcium carbonate to depress the decrease in pH in the capsules. L. fructivorans NRIC0224 and 1-decanol were selected as the Hiochi bacterium and the diluent, respectively, based on the tolerance of aliphatic alcohol and extractability. We found that the presence of powdered CaCO3 in the medium considerably alleviated the toxicity of tri-n-octylamine (TOA) and that the components in the medium, yeast extract and peptone, affected the extraction of lactic acid with TOA in 1-decanol. Then, we co-immobilized both L. fructivorans NRIC0224 cells and CaCO3 into Ca-alginate capsules and constructed an in situ extractive fermentation system using TOA and the Ca-alginate capsules. This system operated successfully, and the yield and productivity were improved over those of control fermentation.