Structural studies of Myceliophthora Thermophila Laccase in the presence of deep eutectic solvents

被引:21
|
作者
Chan, Jou Chin [1 ]
Zhang, Bixia [2 ]
Martinez, Michael [2 ]
Kuruba, Balaganesh [1 ]
Brozik, James [2 ]
Kang, ChulHee [2 ]
Zhang, Xiao [1 ,3 ]
机构
[1] Washington State Univ, Voiland Sch Chem Engn & Bioengn, 2710 Crimson Way, Richland, WA 99354 USA
[2] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[3] Pacific Northwest Natl Lab, 902 Battelle Blvd,POB 999,MSIN P8-60, Richland, WA 99352 USA
基金
美国国家科学基金会;
关键词
Laccase; Deep eutectic solvent; Crystallization; CRYSTAL-STRUCTURE; FUNGAL LACCASES; CHOLINE CHLORIDE; PROTEIN; WATER; STABILITY; MECHANISM; DYNAMICS; INSIGHTS; ENZYMES;
D O I
10.1016/j.enzmictec.2021.109890
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this work, we elucidated the interactions between Myceliophthora thermophila laccase and deep eutectic solvent (DES) by crystallographic and kinetics analyses. Four types of DESs with different hydrogen bond acceptor (HBA) and hydrogen bond donor (HBD), including lactic acid: betaine, glycerol: choline chloride, lactic acid: choline chloride and glycerol: betaine was used. The results revealed that different DES have different effects on laccase activity. Lactic acid-betaine (2:1) DES has shown to enhance laccase activity up to 300 % at a concentration ranged from 2% to 8% v/v, while glycerol: choline chloride and lactic acid: choline chloride DES choline chloride-based DES have found to possess inhibitory effects on laccase under the same concentration range. Detailed kinetic study showed that glycerol: choline chloride DES is a S-parabolic-I-parabolic mixed noncompetitive inhibitor, where conformational changes can occur. The crystal structures of laccase with lactic acid: choline chloride DES (LCDES) were obtained at 1.6 angstrom. Crystallographic analysis suggested that the addition of LCDES causes changes in the laccase active site, but the increase in water molecules observed in the resulting crystal prevented laccase from experiencing drastic structural change. Fluorescence and circular dichroism spectroscopies were also applied to determine the effects of DES on the structural conformation of laccase. The results have confirmed that the presence of DES can trigger changes in the local environments of the amino acids in the active site of laccase which contributes to the changes in its activity and stability.
引用
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页数:11
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