Efficient immobilized phospholipase A1 on Mo‐basing nanomaterials for enzymatic degumming

水解 吸附 化学 两亲性 纳米材料 基质(水族馆) 固定化酶 磷脂酶A1 双水相体系 磷脂酶 化学工程 色谱法 相(物质) 有机化学 地质学 工程类 海洋学 聚合物 共聚物
作者
Duanhao Wang,Meijing Guo,Jiachen Li,Binglin Li,Jiao Wang
出处
期刊:Biotechnology Progress [American Chemical Society]
卷期号:38 (4) 被引量:3
标识
DOI:10.1002/btpr.3256
摘要

Six kinds of Mo-basing nanomaterials (MoO3 , MoO3 @Ru, Mo-PDA, MoPC , MoP, CNT@MoS2 ) were successfully synthesized, which were employed as carriers to immobilize phospholipase A1 (PLA1) for the hydrolysis of phospholipids (PLs). PLA1 was immobilized by a simple adsorption-precipitation-cross-linking to form an "enzyme net" covering on nanoparticles. The greatest advantage of these nanoparticles was their strong hydrophilic surface. It not only permitted their dispersion in the aqueous phase, but also showed the strong affinity for PLs in the organic phase, because amphiphilic PLs had the polar head group and higher hydrophilicity than other oils components. Michaelis-Menten analysis revealed that higher catalytic activity and enzyme-substrate affinity were observed in several immobilized PLA1 than its free form. MoO3 was confirmed to be the best candidate for carrier. The highest specific activity of MoO3 -immobilized PLA1 reached 43.1 U/mg, which was about 1.8 times higher than that of free PLA1 (24.4 U/mg). In addition, the stability and recycling were also enhanced. The robust immobilized PLA1 was prepared in this work, showing great potential for the enzymatic degumming.
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