Abdelhamid Sayeda Abdelrazek, Mohamed Sahar S, Abo Elsoud Mostafa M, Selim Manal S, Mounier Marwa M, Eltaher Ashraf, Magdeldin Sameh, Ali Mohamed, Awady Mohamed E El
Microbial Biotechnology Department, National Research Centre, Cairo, Egypt.
Pharmacognosy Department, National Research Centre, Cairo, Egypt.
Probiotics Antimicrob Proteins. 2025 May 5. doi: 10.1007/s12602-025-10539-w.
Microbial polysaccharides are a significant group of functional phytochemicals. Numerous studies have shown the advantageous pharmacological impacts of polysaccharides, including their effectiveness against cancer. A halophilic bacterial strain obtained from coastal sediments produced exopolysaccharides (EPS). The strain was morphologically recognized and further confirmed as Bacillus cereus strain MSS1 using 16S rDNA analysis, with accession number OR133726. The heteropolysaccharides were purified and fractionated with a DEAE-cellulose column, and the preliminary chemical analysis of the most potent fraction (EPSMSS1) indicated that the four different monosaccharides were mannuronic acid, xylose, fructose, and glucuronic acid, with a molar ratio of 1:1:2:0.5, respectively. The highest production was 12.76 g/l using a Box-Behnken design. It showed antibacterial activity, antioxidant activity, and antibiofilm activity. The 3D architecture of the EPSMSS1 of Bacillus cereus strain MSS1 is being described, predicted, and aligned against other bacterial species. These studies offer valuable insights into optimizing efficiency. Therefore, the EPSMSS1 fraction was shown to have anticancer activity and significant anticancer activities in a dose-dependent manner, with an IC50 value of 20.1 µg/ml. Subsequently, various apoptotic markers, such as cytochrome c, BAX, BCl2, and the BAX/BCL2 ratio, were assessed. Our findings demonstrate that EPSMSS1 triggers the activation of apoptotic protein BAX, enhances the generation of cytochrome c, reduces the expression of antiapoptotic protein BCl2, and distorts the BAX/BCL2 ratio in EPSMSS1-treated HCT-116 cells relative to untreated cells. The anticancer efficacy of EPSMSS1 was verified through the assessment of cell cycle progression using flow cytometry. It has been found that EPSMSS1 pauses the cell cycle in the G1/S phase, causing apoptosis. The main motivation behind this study was EPSMSS1, an innovative marine polysaccharide with remarkable biological activity, especially anti-cancer properties.
微生物多糖是一类重要的功能性植物化学物质。大量研究表明了多糖具有有益的药理作用,包括其抗癌功效。从沿海沉积物中获得的一株嗜盐细菌产生了胞外多糖(EPS)。通过形态学识别该菌株,并使用16S rDNA分析进一步确认为蜡样芽孢杆菌菌株MSS1,登录号为OR133726。用DEAE-纤维素柱对杂多糖进行纯化和分级分离,对最有效的级分(EPSMSS1)进行的初步化学分析表明,四种不同的单糖分别是甘露糖醛酸、木糖、果糖和葡萄糖醛酸,摩尔比分别为1:1:2:0.5。使用Box-Behnken设计,最高产量为12.76 g/l。它表现出抗菌活性、抗氧化活性和抗生物膜活性。蜡样芽孢杆菌菌株MSS1的EPSMSS1的三维结构正在被描述、预测,并与其他细菌物种进行比对。这些研究为优化效率提供了有价值的见解。因此,EPSMSS1级分显示出抗癌活性,且具有显著的剂量依赖性抗癌活性,IC50值为20.1 µg/ml。随后,评估了各种凋亡标志物,如细胞色素c、BAX、BCl2和BAX/BCl2比值。我们的研究结果表明,相对于未处理的细胞,EPSMSS1可触发凋亡蛋白BAX的激活,增强细胞色素c的生成,降低抗凋亡蛋白BCl2的表达,并改变EPSMSS1处理的HCT-116细胞中的BAX/BCl2比值。通过使用流式细胞术评估细胞周期进程,验证了EPSMSS1的抗癌功效。已发现EPSMSS1使细胞周期停滞在G1/S期,从而导致细胞凋亡。本研究的主要动机是EPSMSS1,这是一种具有显著生物活性,尤其是抗癌特性的新型海洋多糖。