Yamabhai Montarop, Khamphio Munthipha, Min Thae Thae, Soem Chai Noy, Cuong Nguyen Cao, Aprilia Waheni Rizki, Luesukprasert Krisanai, Teeranitayatarn Karsidete, Maneedaeng Atthaphon, Tuveng Tina R, Lorentzen Silje B, Antonsen Simen, Jitprasertwong Paiboon, Eijsink Vincent G H
Molecular Biotechnology Laboratory, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand.
Molecular Biotechnology Laboratory, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand.
Carbohydr Polym. 2024 Jan 15;324:121546. doi: 10.1016/j.carbpol.2023.121546. Epub 2023 Nov 2.
Bioconversion of chitosan into soluble anti-inflammatory chitosan oligosaccharides (CHOS) using a Bacillus chitosanase, BsCsn46A, was investigated, including food-grade approaches. After 48 h of enzymatic reaction, most of the final products were dimers and trimers. None of the CHOS products showed toxicity to human fibroblasts. Analysis of CHOS bioactivity against LPS-induced inflammation of human macrophages indicated that CHOS generated from different bioconversion processes have anti-inflammatory activity, the magnitude of which depends on the type of substrate and production process. Both lactic acid and HCl can be used to dissolve chitosan; however, the product generated from lactic acid solution was highly hygroscopic after lyophilization, hence not suitable for long-term storage. Downstream processes, i.e., centrifugation and filtration, affect its anti-inflammatory activity. Analysis of standard CHOS with known structure showed that an acetyl group at the reducing end and the degree of polymerization (DP) are critical for biological activity. Importantly, when applied at levels above the optimal concentrations, certain standard CHOS and CHOS mixtures could induce inflammation. These results support the potential of CHOS as anti-inflammatory agents but reveal batch-to-batch variation and possible side effects, indicating that careful quality assurance of CHOS preparations is essential.
研究了使用壳聚糖酶BsCsn46A将壳聚糖生物转化为可溶性抗炎壳寡糖(CHOS)的过程,包括食品级方法。酶促反应48小时后,最终产物大多为二聚体和三聚体。所有CHOS产物均对人成纤维细胞无毒性。对CHOS针对脂多糖诱导的人巨噬细胞炎症的生物活性分析表明,不同生物转化过程产生的CHOS具有抗炎活性,其强度取决于底物类型和生产过程。乳酸和盐酸均可用于溶解壳聚糖;然而,乳酸溶液产生的产物冻干后吸湿性很强,因此不适合长期储存。下游工艺,即离心和过滤,会影响其抗炎活性。对具有已知结构的标准CHOS分析表明,还原端的乙酰基和聚合度(DP)对生物活性至关重要。重要的是,当以高于最佳浓度的水平应用时,某些标准CHOS和CHOS混合物可能会诱发炎症。这些结果支持了CHOS作为抗炎剂的潜力,但揭示了批次间的差异和可能的副作用,表明对CHOS制剂进行仔细的质量保证至关重要。