Mergulhão Filipe J M, Monteiro Gabriel A, Larsson Gen, Bostrom Maria, Farewell Anne, Nyström Thomas, Cabral Joaquim M S, Taipa M Angela
Centre for Biological and Chemical Engineering, Instituto Superior Técnico, Av. Rovisco Pais, 1049-001 Lisbon, Portugal.
Biotechnol Appl Biochem. 2003 Aug;38(Pt 1):87-93. doi: 10.1042/BA20030043.
Four inducible promoters, uspA, uspB, lacUV5 and malK, were evaluated in the expression of the fusion protein ZZ-proinsulin by Escherichia coli. The aim was to select for their effects on the most appropriate expression system (promoter and culture medium) for secretion of ZZ-proinsulin to the periplasmic space and culture medium. All the expression vectors contained the RNase III cleavage site to ensure that the mRNA translation rate remained independent of 5'-untranslated regions thus making promoter strength comparisons more accurate. The highest ZZ-proinsulin secretion yields were 6.2 mg/g of dry cell weight in the periplasmic space and 2.6 mg/g of dry cell weight in the culture medium using the malK promoter. It was also demonstrated that the use of M9 minimal medium favours secretion.
在大肠杆菌中表达融合蛋白ZZ-胰岛素原时,对四个诱导型启动子uspA、uspB、lacUV5和malK进行了评估。目的是根据它们对最适合的表达系统(启动子和培养基)的影响来选择,以便将ZZ-胰岛素原分泌到周质空间和培养基中。所有表达载体都含有RNase III切割位点,以确保mRNA翻译速率与5'非翻译区无关,从而使启动子强度比较更准确。使用malK启动子时,周质空间中ZZ-胰岛素原的最高分泌产量为6.2 mg/g干细胞重量,培养基中为2.6 mg/g干细胞重量。还证明使用M9基本培养基有利于分泌。