Akroyd J, Symonds N
Gene. 1986;49(2):273-82. doi: 10.1016/0378-1119(86)90288-x.
Using cloning techniques in conjunction with an in vitro assay for activity of the gam-coded protein (pgam), the gam gene has been located on a 930-bp fragment immediately to the right of an AccI site situated 5.75 kb from the left-hand end of the phage Mu genome. An analysis of the properties of pgam obtained from an overproducing clone indicates that it is a non-specific DNA-binding protein which interacts with linear duplex plasmid DNA having a variety of different termini and confers protection against exonuclease action (Gam function). It also stimulates the frequency with which linear plasmid DNA transforms Escherichia coli to antibiotic resistance (Sot function). The preliminary results reported here suggest that pgam is potentially a useful 'tool' in molecular biology, although the molecular details of pgam activity require further clarification.
通过将克隆技术与gam编码蛋白(pgam)活性的体外测定相结合,gam基因已定位在一个930碱基对的片段上,该片段紧邻一个AccI位点的右侧,该AccI位点位于噬菌体Mu基因组左端5.75 kb处。对从一个高产克隆中获得的pgam的特性分析表明,它是一种非特异性DNA结合蛋白,可与具有多种不同末端的线性双链质粒DNA相互作用,并赋予对外切核酸酶作用的抗性(Gam功能)。它还能刺激线性质粒DNA将大肠杆菌转化为抗生素抗性的频率(Sot功能)。此处报道的初步结果表明,尽管pgam活性的分子细节需要进一步阐明,但pgam在分子生物学中可能是一种有用的“工具”。