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食品级蛋白质生产的先进策略:一种用于改进克隆和食品级表达的新型乳酸菌穿梭载体。

Advanced Strategies for Food-Grade Protein Production: A New /Lactic Acid Bacteria Shuttle Vector for Improved Cloning and Food-Grade Expression.

作者信息

Tagliavia Marcello, Nicosia Aldo

机构信息

National Research Council-Institute for the Study of Anthropic Impacts and Sustainability in the Marine Environment (IAS-CNR), Capo Granitola, Via del mare, Campobello di Mazara (TP), 91021 Sicily, Italy.

Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Viale delle Scienze, Ed.16, 90128 Palermo, Italy.

出版信息

Microorganisms. 2019 Apr 27;7(5):116. doi: 10.3390/microorganisms7050116.

Abstract

Food-grade production of recombinant proteins in Gram-positive bacteria, especially in LAB (i.e., , and ), is of great interest in the areas of recombinant enzyme production, industrial food fermentation, gene and metabolic engineering, as well as antigen delivery for oral vaccination. Food-grade expression relies on hosts generally considered as safe organisms and on clone selection not dependent on antibiotic markers, which limit the overall DNA manipulation workflow, as it can be carried out only in the expression host and not in . Moreover, many commercial expression vectors lack useful elements for protein purification. We constructed a "shuttle" vector containing a removable selective marker, which allows feasible cloning steps in and subsequent protein expression in LAB. In fact, the cassette can be easily excised from the selected recombinant plasmid, and the resulting marker-free vector transformed into the final LAB host. Further useful elements, as improved MCS, 6xHis-Tag, and thrombin cleavage site sequences were introduced. The resulting vector allows easy cloning in , can be quickly converted in a food-grade expression vector and harbors additional elements for improved recombinant protein purification. Overall, such features make the new vector an improved tool for food-grade expression.

摘要

在革兰氏阳性菌中,特别是在乳酸菌(即嗜酸乳杆菌、干酪乳杆菌和植物乳杆菌)中进行重组蛋白的食品级生产,在重组酶生产、工业食品发酵、基因与代谢工程以及口服疫苗的抗原递送等领域具有重大意义。食品级表达依赖于通常被视为安全的宿主生物体以及不依赖抗生素标记的克隆选择,这限制了整体的DNA操作流程,因为它只能在表达宿主中进行,而不能在大肠杆菌中进行。此外,许多商业表达载体缺乏用于蛋白质纯化的有用元件。我们构建了一种含有可去除选择标记的“穿梭”载体,该载体允许在大肠杆菌中进行可行的克隆步骤,并随后在乳酸菌中进行蛋白质表达。实际上,该盒式结构可以很容易地从所选重组质粒中切除,并且所得的无标记载体可转化到最终的乳酸菌宿主中。还引入了其他有用元件,如改进的多克隆位点(MCS)、6xHis标签和凝血酶切割位点序列。所得载体便于在大肠杆菌中克隆,可快速转化为食品级表达载体,并含有用于改进重组蛋白纯化的其他元件。总体而言,这些特性使新载体成为食品级表达的一种改进工具。

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