Laboratory of Nano & Biotechnology, Institute of Tropical Pathology and Public Health, Universidade Federal de Goiás, Setor Universitário, Rua 235, s/n, Goiânia, GO, 74605-050, Brazil.
Laboratory of Pathogenic Dimorphic Fungi, Department of Microbiology, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, 05508-000, Brazil.
Folia Microbiol (Praha). 2022 Dec;67(6):935-945. doi: 10.1007/s12223-022-00992-3. Epub 2022 Jul 18.
The accumulation of chitin waste from the seafood industry is a serious environmental problem. However, this residue can be degraded by chitinases and its subproducts, such as chitosan, economically exploited. In this study, a chitinase producer bacteria, identified as Paenibacillus illinoisensis, was isolated from the Brazilian coastal city of Terra de Areia - Rio Grande Do Sul (RS) and was immobilized within alginate beads to evaluate its chitinase production. The alginate beads containing cells presented an average size of 4 mm, 99% of immobilization efficiency and increased the enzymatic activity in 40.71% compared to the free cells. The biomass during enzymatic production increased 62.01% and the total cells leaked from the alginate beads corresponded to 6.46% after 96 h. Immobilized cells were reused in a sequential batch system and remained stable for production for up to four 96-h cycles, decreasing only 21.04% of the initial activity at the end of the fourth cycle. Therefore, the methodology used for cell immobilization resulted in adequate beads to maintain cell viability during the enzymatic production, increasing enzymatic activity, showing low cell leakage from the support and appropriate recyclable capacity.
海鲜加工业产生的大量甲壳素废物是一个严重的环境问题。然而,这种残余物可以通过甲壳素酶及其副产物壳聚糖进行降解,并进行经济开发。在这项研究中,从巴西沿海城市Terra de Areia-Rio Grande do Sul (RS) 分离出一种产甲壳素酶的细菌,鉴定为解淀粉芽孢杆菌,并将其固定在海藻酸钠珠中以评估其甲壳素酶的生产。含有细胞的海藻酸钠珠的平均粒径为 4mm,固定化效率为 99%,与游离细胞相比,酶活性提高了 40.71%。在酶生产过程中,生物量增加了 62.01%,从海藻酸钠珠中泄漏的总细胞在 96 小时后达到 6.46%。固定化细胞在连续分批系统中重复使用,在四个 96 小时的周期内保持稳定,在第四个周期结束时仅降低了 21.04%的初始活性。因此,所采用的细胞固定化方法产生了适当的珠体,以在酶生产过程中维持细胞活力,提高酶活性,显示出从载体中低漏出的细胞和适当的可回收能力。