Gupta M, Carr N G
J Gen Microbiol. 1983 Aug;129(8):2359-66. doi: 10.1099/00221287-129-8-2359.
A method has been established which isolated polysomes from the lysozyme/EDTA-shocked cyanobacterium, Nostoc sp. MAC. In a typical preparation the total recovery of RNA as polysomes was 83%, in which 77% of the polysome fraction was present at sizes greater than 5-mers and 23% as 2-4-mers. Messenger RNA isolated from such a preparation of polysomes produced a 10-fold stimulation in the incorporation of [35S]methionine into polypeptides by a cell-free system of Escherichia coli. The in vitro-synthesized polypeptides were analysed on an SDS-polyacrylamide gradient gel together with in vivo-labelled proteins of Nostoc sp. MAC: seven polypeptides co-migrated with the in vivo-synthesized products. This is the first report of the expression of cyanobacterial messenger RNA in a heterologous cell-free system from E. coli; the efficiency of the system is discussed.
已经建立了一种从溶菌酶/乙二胺四乙酸(EDTA)冲击的蓝细菌念珠藻属(Nostoc sp.)MAC中分离多核糖体的方法。在典型的制备过程中,作为多核糖体的RNA总回收率为83%,其中77%的多核糖体部分以大于五聚体的大小存在,23%为二聚体至四聚体。从这种多核糖体制备物中分离的信使核糖核酸(mRNA)在大肠杆菌无细胞系统中使[35S]甲硫氨酸掺入多肽的过程中产生了10倍的刺激作用。将体外合成的多肽与念珠藻属MAC的体内标记蛋白质一起在十二烷基硫酸钠-聚丙烯酰胺梯度凝胶上进行分析:七种多肽与体内合成产物共迁移。这是关于蓝细菌信使核糖核酸在来自大肠杆菌的异源无细胞系统中表达的首次报道;并对该系统的效率进行了讨论。