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天蓝色链霉菌A3(2)来源的β-琼脂酶制剂的安全性评估

Safety evaluation of β-agarase preparations from Streptomyces coelicolor A3(2).

作者信息

Hong Sun Joo, Lee Je-Hyeon, Kim Eun Joo, Lee Yeon Hee, Jung Hoe Myung, Hong Soon-Kwang

机构信息

Department of Biological Science and Bioinformatics, Myongji University, 116 Myongji-Ro, Cheoin-gu, Yongin, Gyeonggido, 17058, Republic of Korea; Dynebio Inc, B-B205 Woolimlions Valley II, 146-8, Sangdaewon-Dong, Jungwon-Gu, Seongnam-Si, Gyeonggi-Do, 462-807, South Korea.

Dynebio Inc, B-B205 Woolimlions Valley II, 146-8, Sangdaewon-Dong, Jungwon-Gu, Seongnam-Si, Gyeonggi-Do, 462-807, South Korea.

出版信息

Regul Toxicol Pharmacol. 2019 Feb;101:142-155. doi: 10.1016/j.yrtph.2018.11.005. Epub 2018 Nov 16.

Abstract

Recent studies on neoagarooligosaccharides prepared by hydrolyzing agar with β-agarase DagA produced from Streptomyces coelicolor A3(2) have enhanced our knowledge about the enzymatic utility of S. coelicolor. For safety evaluation, a crude extracellular protein containing DagA (crDagA) was prepared from the culture broth of S. coelicolor A3(2) M22-2C43, a highly productive strain of DagA. All genotoxicity tests, such as bacterial reverse mutation assay, eukaryotic chromosomal aberration assay, and in vivo micronucleus assay in mice showed no mutagenic activity of crDagA. No abnormalities were found in the appearance or behavior upon single oral administration up to 20,000 mg/kg body weight (BW) [318 mg TOS (Total Organic Solids)/kg BW] and long-term repeated oral administration toxicity tests up to 10,000 mg/kg BW/day (159 mg TOS/kg BW/day) in Sprague Dawley™ rats. In addition, there were no statistically significant differences in the body weight change, food intake, hematology, blood biochemistry, organ weight, and clinical signs between the crDagA-administered and non-administered groups during the experimental period. This result showed that crDagA produced from S. coelicolor A3(2) is a safe, non-toxic substance, and therefore, can be used safely for manufacturing neoagarooligosaccharide, a functional substance effective in improving metabolic syndrome.

摘要

最近关于用天蓝色链霉菌A3(2)产生的β-琼胶酶DagA水解琼脂制备新琼脂寡糖的研究,增进了我们对天蓝色链霉菌酶学效用的了解。为进行安全性评估,从高产DagA的天蓝色链霉菌A3(2) M22-2C43的培养液中制备了含DagA的粗细胞外蛋白(crDagA)。所有遗传毒性试验,如细菌回复突变试验、真核染色体畸变试验以及小鼠体内微核试验,均显示crDagA无诱变活性。在Sprague Dawley™大鼠中,单次口服高达20,000 mg/kg体重(BW)[318 mg总有机固体(TOS)/kg BW]以及长期重复口服高达10,000 mg/kg BW/天(159 mg TOS/kg BW/天)后,在外观或行为上均未发现异常。此外,在实验期间,给予crDagA组和未给予组之间在体重变化、食物摄入量、血液学、血液生化、器官重量和临床体征方面均无统计学显著差异。该结果表明,从天蓝色链霉菌A3(2)产生的crDagA是一种安全、无毒的物质,因此可安全用于制造新琼脂寡糖,一种对改善代谢综合征有效的功能性物质。

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