Mazotto Ana Maria, Cedrola Sabrina M L, de Souza Edilma P, Couri Sonia, Vermelho Alane B
Laboratory of Microbial Biocatalysis, General Microbiology Department, Microbiology Institute, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 21941-902 Brazil.
Biotechnology Lab-Bioinovar, General Microbiology Department, Microbiology Institute, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 21941-902 Brazil.
3 Biotech. 2022 Apr;12(4):90. doi: 10.1007/s13205-022-03153-y. Epub 2022 Mar 11.
The poultry industry produces millions of tons of feathers waste that can be transformed into valuable products through bioprocess. The study describes the enhanced keratinase and feather hydrolysate production by AMR. The metabolism of each microorganism is unique, so optimization tools are essential to determine the best fermentation parameters to obtain the best process performance. The evaluation of different propagation media indicated the constitutive production of two keratinases of approximately 80 kDa. The combination of Mn, Ca, and Mg at 0.5 mM improved the keratinolytic activity and feather degradation 1.5-fold, while Cu inhibited the enzymatic activity completely. Replace yeast extract for sucrose increased the feather hydrolysate production three times. The best feather concentration for hydrolysate production was 1.5% with an inoculum of 10 CFU/mL and incubation at 30 °C. None of the inorganic additional nitrogen sources tested increased hydrolysate production, although (NH)SO and KNO improved enzymatic activity. The optimization process improved keratinolytic activity from 205.4 to 418.7 U/mL, the protein concentration reached 10.1 mg/mL from an initial concentration of 3.9 mg/mL, and the feather degradation improved from 70 to 96%. This study characterized keratinase and feather hydrolysate production conditions offering valuable information for exploring and utilizing AMR keratinolytic strain for feather valorization.
The online version contains supplementary material available at 10.1007/s13205-022-03153-y.
家禽业产生数百万吨羽毛废弃物,这些废弃物可通过生物工艺转化为有价值的产品。该研究描述了嗜麦芽窄食单胞菌增强角蛋白酶和羽毛水解产物的生产情况。每种微生物的代谢都是独特的,因此优化工具对于确定最佳发酵参数以获得最佳工艺性能至关重要。对不同增殖培养基的评估表明,组成型产生了两种约80 kDa的角蛋白酶。0.5 mM的锰、钙和镁的组合将角蛋白分解活性和羽毛降解提高了1.5倍,而铜则完全抑制了酶活性。用蔗糖替代酵母提取物使羽毛水解产物的产量增加了三倍。水解产物生产的最佳羽毛浓度为1.5%,接种量为10 CFU/mL,在30°C下培养。尽管硫酸铵和硝酸钾提高了酶活性,但测试的无机额外氮源均未增加水解产物的产量。优化过程将角蛋白分解活性从205.4 U/mL提高到418.7 U/mL,蛋白质浓度从初始浓度3.9 mg/mL达到10.1 mg/mL,羽毛降解率从70%提高到96%。本研究表征了角蛋白酶和羽毛水解产物的生产条件,为探索和利用嗜麦芽窄食单胞菌角蛋白分解菌株进行羽毛增值提供了有价值的信息。
在线版本包含可在10.1007/s13205-022-03153-y获取的补充材料。