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利用生物工程益生菌生产植酸酶,降解家禽消化道中的植酸磷。

Production of Phytase Enzyme by a Bioengineered Probiotic for Degrading of Phytate Phosphorus in the Digestive Tract of Poultry.

机构信息

Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.

出版信息

Probiotics Antimicrob Proteins. 2019 Jun;11(2):580-587. doi: 10.1007/s12602-018-9423-x.

Abstract

Probiotics are beneficial microorganisms and have long been used in food production as well as health promotion products. Bioengineered probiotics are used to express and transfer native or recombinant molecules to the mucosal surface of the digestive tract to improve feed efficiency and promote health. Lactococcus lactis is a potential probiotic candidate to produce useful biological proteins. The aim of this investigation was to develop a recombinant Lactococcus lactis with the potential of producing phytase. To enhance the efficiency of expression and secretion of recombinant phytase, usp45 signal peptide was added to the expression vector containing phytase gene (appA2) derived from Escherichia coli. Sequencing of recombinant plasmid containing appA2 showed the correct construction of plasmid. Total length of the phytase insert was 1.25 kbp. A Blast search of the cloned fragment showed 99% similarity to the reported E. coli phytase sequence in the GenBank (accession number: AM946981.2). A plasmid containing usp45 and appA2 electrotransferred into Lactococcus lactis. Zymogram with polyacrylamide gel revealed that the protein extract from the supernatant and the cell pellet of recombinant bacteria had phytase activity. Enzyme activity of 4 U/ml was obtained in cell extracts, and supernatant maximal phytase activity was 19 U/ml. The recombinant L. lactis was supplemented in broiler chicken feed and showed the increase of apparent digestibility on phytate phosphorus in the digestive tract and it was same as performance of E. coli commercial phytase.

摘要

益生菌是有益的微生物,长期以来一直被用于食品生产和促进健康的产品。生物工程益生菌用于表达和转移天然或重组分子到消化道的黏膜表面,以提高饲料效率和促进健康。乳球菌是生产有用生物蛋白的潜在益生菌候选物。本研究的目的是开发一种具有产生植酸酶潜力的重组乳球菌。为了提高重组植酸酶的表达和分泌效率,在含有植酸酶基因(appA2)的表达载体中添加了usp45 信号肽,该基因来自大肠杆菌。含有 appA2 的重组质粒的测序显示质粒的正确构建。植酸酶插入物的全长为 1.25 kbp。克隆片段的 Blast 搜索显示,与 GenBank 中报道的大肠杆菌植酸酶序列(登录号:AM946981.2)有 99%的相似性。含有 usp45 和 appA2 的质粒电转入乳球菌。聚丙烯酰胺凝胶的同工酶显示,重组菌的上清液和细胞沉淀中的蛋白提取物具有植酸酶活性。细胞提取物中获得 4 U/ml 的酶活性,上清液中最大植酸酶活性为 19 U/ml。重组乳球菌补充到肉鸡饲料中,显示出在消化道中植酸磷的表观消化率增加,与大肠杆菌商业植酸酶的性能相同。

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