
pmid: 33233577
pmc: PMC7699763
Microbial fermentation of by-products is a renewable and efficient technique in the development of a range of useful products. In this study, protease synthesis by Paenibacillus sp. TKU052 was carried out on culture media containing some common seafood processing by-products (SPBPs) as the sole source of carbon and nitrogen (C/N). The most suitable C/N nutrition source for the production of proteases was found to be 3.0% (w/v) demineralized crab shells powder (deCSP) and maximal enzyme activity of 4.41 ± 0.16 U/mL was detected on the third day of the culture. Two proteases (P1 and P2) with a similar molecular weight of 31 kDa were successfully isolated and purified from the 3-day deCSP-containing medium. Both P1 and P2 exhibited the highest activity of gelatin hydrolysis at pH 6 and 60 °C. The gelatin hydrolysates catalyzed by Paenibacillus TKU052 proteases were evaluated for biological activities, including 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, angiotensin-I converting enzyme (ACE) inhibition, and prebiotic activities. The gelatin hydrolysates expressed 31.76–43.95% DPPH radical scavenging activity and 31.58–36.84% ACE inhibitory activity, which was higher than those from gelatin. Gelatin hydrolysates also showed the growth-enhancing effect on Bifidobacterium bifidum BCRC 14615 with an increase to 135.70–147.81%. In short, Paenibacillus sp. TKU052 could be a potential strain to utilize crab shell wastes to produce proteases for bio-active peptides’ preparation.
Food Handling, Protein Hydrolysates, Angiotensin-Converting Enzyme Inhibitors, Biochemistry, Gene, Antioxidants, angiotensin-I converting enzyme inhibitory activity;free radical scavenging activity;Paenibacillus;peptide;prebiotic;protease, Substrate Specificity, Agricultural and Biological Sciences, Food science, Enzyme Stability, Biology (General), Hydrolysis, Probiotics and Prebiotics, Life Sciences, Proteases, peptide, Chemistry, prebiotic, Antioxidant, Paenibacillus, Biotechnology, 16S ribosomal RNA, 570, QH301-705.5, Brachyura, 610, free radical scavenging activity, Hydrolysate, Article, Industrial Microbiology, Bacterial Proteins, Animal Shells, Biochemistry, Genetics and Molecular Biology, angiotensin-I converting enzyme inhibitory activity, Animals, <i>Paenibacillus</i>, Molecular Biology, Waste Products, protease, Protease, Bioactive Peptides in Food and Health, Prebiotics, Seafood, Enzyme, Proteolysis, Fermentation, Microbial Enzymes and Biotechnological Applications, Gelatin, Peptides, Peptide Hydrolases, Food Science, DPPH
Food Handling, Protein Hydrolysates, Angiotensin-Converting Enzyme Inhibitors, Biochemistry, Gene, Antioxidants, angiotensin-I converting enzyme inhibitory activity;free radical scavenging activity;Paenibacillus;peptide;prebiotic;protease, Substrate Specificity, Agricultural and Biological Sciences, Food science, Enzyme Stability, Biology (General), Hydrolysis, Probiotics and Prebiotics, Life Sciences, Proteases, peptide, Chemistry, prebiotic, Antioxidant, Paenibacillus, Biotechnology, 16S ribosomal RNA, 570, QH301-705.5, Brachyura, 610, free radical scavenging activity, Hydrolysate, Article, Industrial Microbiology, Bacterial Proteins, Animal Shells, Biochemistry, Genetics and Molecular Biology, angiotensin-I converting enzyme inhibitory activity, Animals, <i>Paenibacillus</i>, Molecular Biology, Waste Products, protease, Protease, Bioactive Peptides in Food and Health, Prebiotics, Seafood, Enzyme, Proteolysis, Fermentation, Microbial Enzymes and Biotechnological Applications, Gelatin, Peptides, Peptide Hydrolases, Food Science, DPPH
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