Studies on the digestive protease of Spilosoma obliqua.
thesis.pdf - Munin Identification, Cloning and Expressions of Proteases from a Cold .
Protease activity was optimum at pH 8.0 and 60°C.
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PhD thesis, Alkaline proteases: A review 183 Optimization of alkaline protease production by Bacillus Declaration I declare that, this thesis entitled “ Optimization of alkaline protease production by Bacillus licheniformis MZK05M9 in batch culture using Response Optimization of Protease Enzyme Production Using Bacillus Sp Optimization of Protease Enzyme Production carbon and nitrogen can influence protease enzymeAssay for Protease: The enzyme was assayed in the Isolation, production and characterization of protease from Isolation, production and characterization of protease from Fig.
In all cases, pH 7 was the optimum for production of protease.
It is clear from our extensive clinical experience that pancreatic proteolytic enzymes have a profound anti-neoplastic effect, but we do not know how they work. We have not had the resources to support basic science research, but with appropriate funding we do not believe it would difficult to set up animal models to explore the molecular action of the enzymes against cancer cells.
I began researching the use of oral pancreatic proteolytic enzyme therapy as a treatment for cancer after completion of my second year at Cornell University Medical College in 1981. My research advisor at the time supported and directed my early work, and later supported me during my formal immunology fellowship. In terms of the theoretical foundation, the exact mechanism of action has never been demonstrated. After Beards death, the enzyme therapy was largely forgotten and certainly never generated any significant research effort until recently with the funding of my work. There are several studies from the 1960s showing, in an animal model, that orally ingested pancreatic enzymes have an anti-cancer effect, and might work through immune modulation, but these studies were preliminary and were never followed-up. Dr. Beard believed enzymes had to be injected to prevent destruction by hydrochloric acid in the stomach. However, recent evidence demonstrates that orally ingested pancreatic proteolytic enzymes are acid stable, pass intact into the small intestine and are absorbed through the intestinal mucosa into the blood stream as part of an enteropancreatic recycling process.
Optimization of the Growth Conditions for Production of Protease
shows that YPTD medium exhibited the highest F1 protease expression as compared to other suggested media. Tryptic soy broth (TSB) was used as nitrogen source instead of yeast nitrogen base (YNB). TSB was much more economical as compared to YNB. On the other hand, YPG showed lower expression level as compared to YPD where the glycerol was not preferable for GAP regulation system. Furthermore, BMDH could not be used as production medium when there were no peptone and yeast extract to generate mass and energy. Yeast extract could increase the recombinant protein secretion and accumulation ().
Recombinant GE6GS was selected for optimization study where it was cultivated in various media composition containing different nitrogen and carbon sources to be used in protein expression. BMD, BMDH and YPTD were modified from BMGY, BMGH and YPTG media, respectively. Glycerol in each medium was replaced with dextrose. Glycerol was used to generate cell mass when using inducible AOX1 expression system. No inducer was needed for GAP expression, therefore, dextrose was chosen as the carbon source. Buffered medium was used to control the pH of the culture (EasySelectTM Expression Kit manual). In addition, when the pH was being controlled, native protease expression from the host was decreased. BYPD was used by to express the antifreeze protein. YPG was modified from YPD medium to see the effect of glycerol on F1 protease expression under regulation GAP promoter. suggested that YPTM medium was the best medium for L2 lipase production under the control of AOX promoter. Therefore, YPTD was generated by replacing the 0.5% (v/v) methanol with 1% (w/v) dextrose.
Use of Agro-industrial Wastes as Substrates for Protease Production
Screening to Optimize Protease Producing Isolates
This essay has been submitted by a Purification and characterization of thermophilic alkaline protease.
Optimization of Protease Production
This essay has been submitted by a Alkaline proteases: A review Enzyme-assisted de-hairing is Anwar, A.
Proteases are obtained from plant, animal and microbial sources.
Proteases are widely distributed in microbial populations viz.
Studies on the effect of concentration of divalent ions revealed that both the activity and stability of protease were better in 1 mM than in 5 mM concentration.
Biotechnological production of alkaline protease for industrial use.
Pre-incubation at temperatures above 70°C for PS-3 and PI-3 and 50°C for PM-1 resulted in reduction of enzyme activity, indicating that the proteases are thermally unstable.
Molecular and biotechnological aspects of microbial proteases.
Furthermore, evaluation of some agro-industrial wastes as potential substrates for protease production indicated that wheat bran was better for PS-3 (4.3 U/ml) and PM-1 (3.0 U/ml), whereas human hair was better for PI-3 (3.9 U/ml).
Alkaline protease production from alkalophilic sp.
Since protease was produced from readily available complex substrates and agro-industrial wastes, the 3 Bacillus species appear to have substantial potential for application in various proteolytic processes.
Screening of Substrates for Protease Production from
Thus, identification of the 3 Bacillus isolates at a molecular level and purification as well as detailed characterization of the types of the proteases are recommended for effective utilization in different area of applications.
Production of Protease Enzyme from Sm3.
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