Kim Jonghwan, Hwang Su Jung, Lee Gyu Sung, Lee Ju Ryeong, An Hye In, Im Hong Sik, Kim Minji, Lee Sang-Seob, Lee Hyo-Jong, Kim Chung Sub
Department of Biopharmaceutical Convergence, Sungkyunkwan University, Suwon 16419, Republic of Korea.
School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
ACS Omega. 2024 Jul 29;9(32):34259-34267. doi: 10.1021/acsomega.3c09585. eCollection 2024 Aug 13.
and are fish gut bacteria that have been isolated from the guts of and , respectively. A total of 22 compounds (-) were isolated from these two bacteria; 16 compounds (-) from and 6 compounds (-) from . Their chemical structures were elucidated by spectroscopic and spectrometric data analysis and chemical synthesis. Compounds and showed strong collagenase inhibitory activity, with 31.91% and 36.43% at 20 μM, respectively, comparable to or surpassing that of the positive control epigallocatechin gallate (EGCG, 34.66%). Also, compounds and exhibited a mild tyrosinase inhibitory effect of 6.73% and 13.68%, respectively. All of the tested compounds displayed no significant antibacterial activity against and up to 100 μM. The collagenase- and tyrosinase-inhibitory compound , cyclo(l-Pro-d-Leu), was found to be stable under heat (50 °C) and UV light (254 and 365 nm) for up to 6 days. These results indicate that compound could be developed into a cosmeceutical with antiaging effects.
[细菌名称1]和[细菌名称2]分别是从[鱼名称1]和[鱼名称2]的肠道中分离出来的鱼肠道细菌。从这两种细菌中总共分离出22种化合物(-);从[细菌名称1]中分离出16种化合物(-),从[细菌名称2]中分离出6种化合物(-)。通过光谱和光谱数据分析以及化学合成阐明了它们的化学结构。化合物[化合物名称1]和[化合物名称2]表现出很强的胶原酶抑制活性,在20μM时分别为31.91%和36.43%,与阳性对照表没食子儿茶素没食子酸酯(EGCG,34.66%)相当或超过其活性。此外,化合物[化合物名称1]和[化合物名称2]分别表现出6.73%和13.68%的轻度酪氨酸酶抑制作用。所有测试化合物在高达100μM时对[细菌名称3]和[细菌名称4]均无显著抗菌活性。发现具有胶原酶和酪氨酸酶抑制作用的化合物[化合物名称3],环(L-脯氨酸-D-亮氨酸),在加热(50°C)和紫外线(254和365nm)下长达6天都是稳定的。这些结果表明化合物[化合物名称3]可以开发成具有抗衰老作用的药妆品。