Linda Tetty Marta, Maisyaroh Dinda Putri, Berlyansah Azizul, Tasliyah Balqis Juanne, Juliantari Erwina, Zul Delita, Fibriarti Bernadeta Leni, Agesti Asih Rahayu Ajeng, Haryani Yuli
Department of Biology, Faculty of Mathematics and Natural Sciences, University of Riau, Kampus Bina Widya Km. 12,5, Simpang Baru Pekanbaru 28293, Indonesia.
Department of Biology Education, Faculty of Teacher Training and Education, University of Riau, Kampus Bina Widya Km. 12,5, Simpang Baru Pekanbaru 28293, Indonesia.
J Microbiol Biotechnol. 2025 Apr 27;35:e2412031. doi: 10.4014/jmb.2412.12031.
Diabetes mellitus (DM) is a primary global health concern, often progressing unnoticed until complications arise. Current antidiabetic therapies primarily aim to inhibit the α-amylase enzyme, thereby reducing blood glucose levels. Some medicinal plants are proven to be symbiotic with endophytic bacteria that produce bioactive compounds capable of inhibiting α-amylase activity. This study investigated the potential of endophytic bacteria isolated from the stem of the sea fern ( L.) to act as α-amylase inhibitors, using both in vitro and in silico studies. Phytochemical analysis of both the stem extract and cultured bacterial isolates showed the presence of alkaloids, flavonoids, and saponins. Isolate B.SB 1.1 was identified as based on 16S rRNA sequencing. The α-amylase inhibition assay demonstrated the strain as showing significant inhibitory activity, with 32.57% inhibition at 2% starch substrate concentration. In silico docking studies using LC-MS data predicted 4-propylbiphenyl and benzoin as compounds with the lowest binding energy to α-amylase, suggesting their potential as effective inhibitors. These findings highlight the efficacy and therapeutic potential of endophytic strain B.SB 1.1 as a novel antidiabetic agent.
糖尿病(DM)是全球主要的健康问题,通常在并发症出现之前未被察觉地发展。目前的抗糖尿病疗法主要旨在抑制α-淀粉酶,从而降低血糖水平。一些药用植物被证明与能产生抑制α-淀粉酶活性的生物活性化合物的内生细菌共生。本研究通过体外和计算机模拟研究,调查了从海蕨(L.)茎中分离出的内生细菌作为α-淀粉酶抑制剂的潜力。对茎提取物和培养的细菌分离物的植物化学分析表明存在生物碱、黄酮类化合物和皂苷。根据16S rRNA测序,分离物B.SB 1.1被鉴定为 。α-淀粉酶抑制试验表明该菌株具有显著的抑制活性,在2%淀粉底物浓度下抑制率为32.57%。使用LC-MS数据进行的计算机模拟对接研究预测4-丙基联苯和安息香是与α-淀粉酶结合能最低的化合物,表明它们作为有效抑制剂的潜力。这些发现突出了内生菌株B.SB 1.1作为新型抗糖尿病药物的功效和治疗潜力。