Protein-Glutaminase Engineering Based on Isothermal Compressibility Perturbation for Enhanced Modification of Soy Protein Isolate

被引:22
作者
Zheng, Nan [1 ]
Long, Mengfei [1 ]
Zhang, Zehua [1 ]
Zan, Qijia [1 ]
Osire, Tolbert [2 ]
Zhou, Huimin [1 ]
Xia, Xiaole [1 ]
机构
[1] Jiangnan Univ, Key Lab Ind Biotechnol, Minist Educ, Sch Biotechnol, Wuxi 214122, Jiangsu, Peoples R China
[2] Shenzhen MSU BIT Univ, Fac Biol, Shenzhen 518172, Guangdong, Peoples R China
基金
中国博士后科学基金;
关键词
protein-glutaminase; isothermal compressibility (?T) perturbation engineering (ICPE) strategy; activity; soy protein isolate (SPI); modification; CHRYSEOBACTERIUM-PROTEOLYTICUM; ENZYMATIC DEAMIDATION; FUNCTIONAL-PROPERTIES; OPTIMIZATION; STABILITY; PRESSURE;
D O I
10.1021/acs.jafc.2c06063
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Protein-glutaminase plays a significant role in future food (e.g., plant-based meat) processing as a result of its ability to improve the solubility, foaming, emulsifying, and gel properties of plant-based proteins. However, poor stability, activity, high pressure, and high shear processing environments hinder its application. Therefore, we developed an application-oriented method isothermal compressibility perturbation engineering strategy to improve enzyme performance by simulating the high-pressure environment. The best variant with remarkable improvement in specific activity and half-time, N16M/Q21H/T113E, exhibited a 4.28-fold increase compared to the wild type in specific activity (117.18 units/mg) and a 1.23-fold increase in half-time (472 min), as one of the highest comprehensive performances ever reported. The solubility of the soy protein isolate deaminated by the N16M/ Q21H/T113E mutant was 55.74% higher than that deaminated by the wild type, with a tinier particle size and coarser texture. Overall, this strategy has the potential to improve the functional performance of enzymes under complex food processing conditions.
引用
收藏
页码:13969 / 13978
页数:10
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