Changing the nutrient composition and enhancing the hydrolytic enzyme activity of citrus pulp residue by cofermentation with Candida utilis and Bacillus subtilis

Author(s):  
Wen-Qi Huang ◽  
Xi Hu ◽  
Jia-Rui Zeng ◽  
Xiao-Fei Tian ◽  
Zhen-Qiang Wu
Polar Biology ◽  
2011 ◽  
Vol 34 (12) ◽  
pp. 2007-2023 ◽  
Author(s):  
Colleen T. E. Kellogg ◽  
Shelly D. Carpenter ◽  
Alisha A. Renfro ◽  
Amélie Sallon ◽  
Christine Michel ◽  
...  

2021 ◽  
Vol 66 (1) ◽  
pp. 72-79
Author(s):  
Thuoc Doan Van ◽  
Hung Nguyen Phuc

The effect of physical parameters such as temperature and pH on the production, activity, and stability of α-amylase from Bacillus subtilis V37 was investigated. The results indicated that the optimum culture conditions for enzyme activity were pH 7.0 and 35 oC. The optimum pH and temperature for enzyme activity were 6.0 and 70 oC. The crude enzyme was found to be stable in the pH range of 5.0 to 7.0. The enzyme was stable for 1 h at a temperature from 30 to 80 oC; nearly 100% of enzyme activity remained at temperatures of 30 - 40 oC, and about 34% of original activity remained at a temperature of 80 oC. These features demonstrated that α-amylase from B. subtilis V37 can be applied in many areas such as the food, fermentation, and animal feed industries.


ACS Sensors ◽  
2018 ◽  
Vol 3 (8) ◽  
pp. 1489-1498 ◽  
Author(s):  
Sadaf Charkhabi ◽  
Andee M. Beierle ◽  
Marshall D. McDaniel ◽  
Nigel F. Reuel

2016 ◽  
Vol 2 (4) ◽  
pp. 402-411 ◽  
Author(s):  
Camilo Muñoz ◽  
◽  
Fernando G. Fermoso ◽  
Mariella Rivas ◽  
Juan M. Gonzalez

2016 ◽  
Vol 14 (38) ◽  
pp. 9146-9150 ◽  
Author(s):  
Anna Żądło-Dobrowolska ◽  
Martyna Szczygieł ◽  
Dominik Koszelewski ◽  
Daniel Paprocki ◽  
Ryszard Ostaszewski

Self-immolative probes for rapid and sensitive hydrolase detection are reported. This system allows hydrolytic enzyme screening through a cascade reaction triggered by enzymatic cleavage.


Author(s):  
ARUN KUMAR ◽  
POONAM KUMARI ◽  
KASAHUN GUDETA ◽  
JM JULKA

Objective: The paper aimed to immobilize amylase producing bacterial strain on a suitable matrix and characterization of its physicochemical properties so that much amount of amylase could be produced to be applied in different industries. Methods: Bacterial colonies were sub-cultured from samples collected from soil in freshly prepared dishes containing starch agar by dot method using sterile inoculating needles from which five different bacteria belonged to genus Bacillus were isolated and assigned as A1, A2, A3, A4, and A5. Results: It was found that A1 displayed the highest enzyme activity of 17.89 IU/ml with enzyme assay of 0.83 mg/ml and the bacterium was identified to be Bacillus subtilis. A5 displayed 10.13 IU/ml with protein contents of 0.11 mg/ml indicated that A1 possess the highest enzyme activities which were categorized under Bacillus and protein contents and A5 showed less amount of enzyme activities and protein contents as compared to other. Conclusion: The bacteria which were produced much amount of enzyme activities identified as Bacillus subtilis and recommended and have been recommended to be cultured for the production of amylase enzyme.


Toxins ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 552 ◽  
Author(s):  
Liu ◽  
Chang ◽  
Wang ◽  
Yin ◽  
Huang ◽  
...  

In order to remove zearalenone (ZEA) detriment—Bacillus subtilis, Candida utilis, and cell-free extracts from Aspergillus oryzae were used to degrade ZEA in this study. The orthogonal experiment in vitro showed that the ZEA degradation rate was 92.27% (p < 0.05) under the conditions that Candida utilis, Bacillus subtilis SP1, and Bacillus subtilis SP2 were mixed together at 0.5%, 1.0%, and 1.0%. When cell-free extracts from Aspergillus oryzae were combined with the above probiotics at a ratio of 2:1 to make mycotoxin-biodegradation preparation (MBP), the ZEA degradation rate reached 95.15% (p < 0.05). In order to further investigate the MBP effect on relieving the negative impact of ZEA for pig production performance, 120 young pigs were randomly divided into 5 groups, with 3 replicates in each group and 8 pigs for each replicate. Group A was given the basal diet with 86.19 μg/kg ZEA; group B contained 300 μg/kg ZEA without MBP addition; and groups C, D, and E contained 300 μg/kg ZEA added with 0.05%, 0.10%, and 0.15% MBP, respectively. The results showed that MBP addition was able to keep gut microbiota stable. ZEA concentrations in jejunal contents in groups A and D were 89.47% and 80.07% lower than that in group B (p < 0.05), indicating that MBP was effective in ZEA biodegradation. In addition, MBP had no significant effect on pig growth, nutrient digestibility, and the relative mRNA abundance of estrogen receptor alpha (ERα) genes in ovaries and the uterus (p > 0.05).


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