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基于DNA技术的胶原蛋白产品鉴定进展。

Advances in the authentication of collagen products based on DNA technology.

作者信息

Chen Yuan, Wang Yang, Ma Chenwei, Li Yangshuai, Zuo Doudou, Huang Xiaoli, Tian Xiaojing, Wang Wenhang

机构信息

College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin, China.

RandD Centre of Collagen Products, Xingjia Biotechnology Co. LTD, Tianjin, China.

出版信息

Crit Rev Food Sci Nutr. 2025;65(5):884-895. doi: 10.1080/10408398.2023.2283278. Epub 2023 Nov 20.

Abstract

Collagenous products are making their way into consumer markets such as foods, nutraceuticals, cosmetics and pharmaceuticals increasingly. Collagen in a large family of proteins is ubiquitous in metazoan. The most effective way to identify biological samples including collagen is DNA technology indisputably. However, the DNA content of collagen mostly derived from connective tissue is relatively less, and commercial collagen products are usually subjected to some harsh treatments in the production process, which makes DNA damage more serious, thus tracing their origin becomes a huge challenge. At present, DNA enrichment mainly relies on silica based centrifugal columns after extraction by classical phenol chloroform method. For improving the amplification of DNA fragments, small amplicons are designed based on more stable mitochondrial genes, such as cytochrome b gene (cytb). In addition to conventional PCR for DNA amplification, some new PCR techniques have also been developed, such as DNA barcoding techniques, PCR-Southern hybridization and fluorescent PCR. These PCR techniques have their pros and cons, and are mainly used in the identification of gelatin at present. The development of a complete set of DNA authentication is of great significance for the control of collagen products quality and will contribute to sustainable development of collagen industry.

摘要

胶原蛋白产品正越来越多地进入食品、营养保健品、化妆品和药品等消费市场。胶原蛋白是一大类蛋白质,在后生动物中普遍存在。毫无疑问,识别包括胶原蛋白在内的生物样本最有效的方法是DNA技术。然而,大部分来源于结缔组织的胶原蛋白的DNA含量相对较少,并且商业胶原蛋白产品在生产过程中通常会经过一些苛刻的处理,这使得DNA损伤更加严重,因此追踪它们的来源成为了一个巨大的挑战。目前,DNA富集主要依靠在通过经典酚氯仿法提取后使用基于硅胶的离心柱。为了提高DNA片段的扩增效果,基于更稳定的线粒体基因(如细胞色素b基因(cytb))设计了小扩增子。除了用于DNA扩增的常规PCR外,还开发了一些新的PCR技术,如DNA条形码技术、PCR- Southern杂交和荧光PCR。这些PCR技术各有优缺点,目前主要用于明胶的鉴定。一套完整的DNA鉴定方法的开发对于胶原蛋白产品质量控制具有重要意义,并将有助于胶原蛋白产业的可持续发展。

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