TY - JOUR
T1 - Separation of 5-aminovalerate from its bioconversion liquid by macroporous adsorption resin
T2 - mechanism and dynamic separation
AU - Xu, Sheng
AU - Lu, Xuedong
AU - Li, Mei
AU - Wang, Jing
AU - Li, Hui
AU - He, Xun
AU - Feng, Jiao
AU - Wu, Jinglan
AU - Chen, Kequan
AU - Ouyang, Pingkai
N1 - Publisher Copyright:
© 2019 Society of Chemical Industry
PY - 2020/3/1
Y1 - 2020/3/1
N2 - BACKGROUND: 5-aminovalerate (5-AVA) is the precursor of valerolactam, a potential building block for producing nylon 5, and also regarded as a potential C5 chemical platform. Although 5-AVA bioproduction has been developed, few studies have emphasized the separation of 5-AVA from the bioconversion liquid. RESULTS: An effective and benign method for separation of 5-AVA from its bioconversion liquid was proposed based on chromatography technology using macroporous adsorption resin AK-1. This work focuses on explosion of the adsorption mechanism and optimization of the operating conditions. Freundlich model and thermodynamics results showed that the adsorption affinity of 5-AVA to the AK-1 resin was weaker than that of l-lysine. Combination of the characterization results of AK-1 resin with the physicochemical properties of 5-AVA and l-lysine, the adsorption mechanism was proposed as meso-micropore diffusion, and hydrogen bonding and hydrophobic effects. In dynamic studies, a 5-AVA purity of 99.3% and yield of 92% was obtained at an operating temperature of 353.15 K on a 40:1 chromatographic column eluted by deionized water. The residual 5-AVA and l-lysine were recovered by 1 mol L–1 HCl, which can be used as a feed material in the 5-AVA conversion process repeatedly. CONCLUSION: An innovative benign efficient environmentally process for recovery of 5-AVA from the bioconversion liquid was developed based on a macroporous resin AK-1. Compared with ion exchange resins, macroporous resins can efficiently adsorb 5-AVA, whereas salt ions cannot be retained. This clean and efficient method provides a promising strategy for separating similar biochemical products.
AB - BACKGROUND: 5-aminovalerate (5-AVA) is the precursor of valerolactam, a potential building block for producing nylon 5, and also regarded as a potential C5 chemical platform. Although 5-AVA bioproduction has been developed, few studies have emphasized the separation of 5-AVA from the bioconversion liquid. RESULTS: An effective and benign method for separation of 5-AVA from its bioconversion liquid was proposed based on chromatography technology using macroporous adsorption resin AK-1. This work focuses on explosion of the adsorption mechanism and optimization of the operating conditions. Freundlich model and thermodynamics results showed that the adsorption affinity of 5-AVA to the AK-1 resin was weaker than that of l-lysine. Combination of the characterization results of AK-1 resin with the physicochemical properties of 5-AVA and l-lysine, the adsorption mechanism was proposed as meso-micropore diffusion, and hydrogen bonding and hydrophobic effects. In dynamic studies, a 5-AVA purity of 99.3% and yield of 92% was obtained at an operating temperature of 353.15 K on a 40:1 chromatographic column eluted by deionized water. The residual 5-AVA and l-lysine were recovered by 1 mol L–1 HCl, which can be used as a feed material in the 5-AVA conversion process repeatedly. CONCLUSION: An innovative benign efficient environmentally process for recovery of 5-AVA from the bioconversion liquid was developed based on a macroporous resin AK-1. Compared with ion exchange resins, macroporous resins can efficiently adsorb 5-AVA, whereas salt ions cannot be retained. This clean and efficient method provides a promising strategy for separating similar biochemical products.
KW - 5-aminovaleric
KW - adsorption mechanism
KW - bioconversion liquid
KW - dynamic separation
KW - macroporous adsorption resin
UR - http://www.scopus.com/inward/record.url?scp=85075727540&partnerID=8YFLogxK
U2 - 10.1002/jctb.6249
DO - 10.1002/jctb.6249
M3 - 文章
AN - SCOPUS:85075727540
SN - 0268-2575
VL - 95
SP - 686
EP - 693
JO - Journal of Chemical Technology and Biotechnology
JF - Journal of Chemical Technology and Biotechnology
IS - 3
ER -