Purification, physico-chemico-kinetic characterization and thermal inactivation thermodynamics of milk clotting enzyme from Bacillus subtilis MTCC 10422

LWT ◽  
2016 ◽  
Vol 65 ◽  
pp. 652-660 ◽  
Author(s):  
Rajesh Kumari Narwal ◽  
Bharat Bhushan ◽  
Ajay Pal ◽  
Anil Panwar ◽  
Sarla Malhotra
2016 ◽  
Vol 15 (3) ◽  
pp. 158 ◽  
Author(s):  
HalaR Wehaidy ◽  
MohamedA Abdel-Naby ◽  
WafaaG Shousha ◽  
MohammedI.Y. El Mallah ◽  
MichaelM Shawky

2018 ◽  
Vol 111 ◽  
pp. 296-301 ◽  
Author(s):  
Hala Refaat Wehaidy ◽  
Mohamed Ahmed Abdel-Naby ◽  
Wafaa Ghoneim Shousha ◽  
Mohammed I.Y. Elmallah ◽  
Michael Mounir Shawky

2018 ◽  
Vol 66 (24) ◽  
pp. 6162-6169 ◽  
Author(s):  
Fanqiang Meng ◽  
Rui Chen ◽  
Xiaoyu Zhu ◽  
Yingjian Lu ◽  
Ting Nie ◽  
...  

2011 ◽  
Vol 10 (46) ◽  
pp. 9370-9378 ◽  
Author(s):  
Ding Zhongyang ◽  
Liu Shuangping ◽  
Gu Zhenghua ◽  
Zhang Liang ◽  
Zhang Kechang ◽  
...  

2002 ◽  
Vol 69 (2) ◽  
pp. 269-279 ◽  
Author(s):  
MAURICE G. HAYES ◽  
JORGE C. OLIVEIRA ◽  
PAUL L. H. McSWEENEY ◽  
ALAN L. KELLY

The aspartic proteinase, chymosin (EC 3.4.23.4) is the principal milk clotting enzyme used in cheese production and is one of the principal proteolytic agents involved in cheese ripening. Varietal differences in chymosin activity, due to factors such as cheese cooking temperature, fundamentally influence cheese characteristics. Furthermore, much chymosin is lost in whey, and further processing of this by-product may require efficient inactivation of this enzyme, with minimal effects on whey proteins. In the first part of this study, the thermal inactivation kinetics of Maxiren 15 (a recombinant chymosin preparation) were studied in skim milk ultrafiltration permeate, whole milk whey and skim milk whey. Inactivation of chymosin in these systems (at pH 6.64) followed first order kinetics with a D45.5 value of 100±21 min and a z-value of 5.9±0.3 °C. D-Values increased linearly with decreasing pH from 6.64 to 6.2, while z-values decreased as pH decreased from 6.64 to 6.4, but were similar at pH 6.4 and 6.2. Subsequent determination of chymosin activity during manufacture of Cheddar and Swiss-type cheese showed good correlations between predicted and experimental values for thermal inactivation of chymosin in whey. However, both types of cheese curd exhibited relatively constant residual chymosin activity throughout manufacture, despite the higher cooking temperature applied in the manufacture of Swiss cheese. Electrophoretic analysis of slurries made from Cheddar and Swiss cheese indicated decreased proteolysis due to chymosin activity during storage of the Swiss cheese slurry, but hydrolysis of sodium caseinate by coagulant extracted from both cheese types indicated similar levels of residual chymosin activity. This may suggest that some form of conformational change other than irreversible thermal denaturation of chymisin takes place in cheese curd during cooking, or that some other physico-chemical difference between Swiss and Cheddar cheese controls the activity of chymosin during ripening.


Author(s):  
D.V. Abramov ◽  
◽  
D.S. Myagkonosov ◽  
I.N. Delitskaya ◽  
V.A. Mordvinova ◽  
...  

2021 ◽  
Vol 69 (9) ◽  
pp. 2784-2792
Author(s):  
Fanqiang Meng ◽  
Haizhen Zhao ◽  
Fengxia Lu ◽  
Xiaomei Bie ◽  
Zhaoxin Lu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document