Corotto L V, Wolber P K, Warren G J
EMBO J. 1986 Feb;5(2):231-6. doi: 10.1002/j.1460-2075.1986.tb04203.x.
A DNA fragment of 7.5 kb from Pseudomonas fluorescens MS1650 confers an ice nucleation phenotype when cloned in Escherichia coli. This DNA encodes a protein with an apparent mol. wt of 180 kd, which is found in both inner and outer membrane fractions of transformed E. coli cells. Insertion mutations throughout a 3.9-kb region cause deficiency in ice nucleation, and eliminate the 180-kd protein. Complementation is not observed between any pair of mutations, suggesting that the nucleating phenotype is encoded by a single transcriptional unit. Mutations in most parts of the 3.9-kb region are not completely deficient in phenotype: they still generate ice nuclei at low frequency. One insertion mutation was found to generate pseudowild revertants, which had undergone deletions of the entire insertion and some of the adjacent sequence; these could account for the incomplete deficiency. These deletions displayed depressed nucleation temperatures, but their nucleation frequencies were close to that of the wild-type gene.
荧光假单胞菌MS1650的一段7.5 kb DNA片段克隆到大肠杆菌中时赋予其冰核形成表型。该DNA编码一种表观分子量为180 kd的蛋白质,在转化的大肠杆菌细胞的内膜和外膜组分中均有发现。整个3.9 kb区域的插入突变导致冰核形成缺陷,并消除180 kd蛋白质。任何一对突变之间均未观察到互补现象,这表明成核表型由单个转录单元编码。3.9 kb区域大部分部位的突变在表型上并非完全缺陷:它们仍能以低频率产生冰核。发现一个插入突变产生了假野生回复体,其整个插入片段和一些相邻序列发生了缺失;这些缺失可以解释不完全缺陷现象。这些缺失表现出较低的成核温度,但其成核频率与野生型基因相近。