Ishiguro N, Sato G
Department of Veterinary Public Health, Obihiro University of Agriculture and Veterinary Medicine, Hokkaido, Japan.
J Bacteriol. 1988 Apr;170(4):1902-6. doi: 10.1128/jb.170.4.1902-1906.1988.
The nucleotide sequences of insertion sequences IS3411L (left) and IS3411R (right), present as direct terminal repeats in the citrate utilization of citrate utilization transposon Tn3411, and of IS3411 (generated by intramolecular recombination between IS3411L and IS3411R) were determined. The three IS3411 elements (IS3411R, IS3411L, and IS3411) were 1,309 base pairs long and identical in DNA sequence. IS3411 had 27-base-pair terminal inverted repeats with three bases mismatched and one long open reading frame (240 amino acids) that was proposed to be a transposase. Three polypeptides of 29,000, 27,000, and about 10,000 molecular weight, determined by IS3411, were identified in minicells. Since Tn3411 generates a 3-base-pair repeat upon integration, the nucleotide sequences of IS3411 were compared with those of IS3.
确定了作为柠檬酸利用转座子Tn3411柠檬酸利用中直接末端重复序列存在的插入序列IS3411L(左)和IS3411R(右)以及IS3411(由IS3411L和IS3411R之间的分子内重组产生)的核苷酸序列。这三个IS3411元件(IS3411R、IS3411L和IS3411)长度为1309个碱基对,DNA序列相同。IS3411具有27个碱基对的末端反向重复序列,有三个碱基错配,还有一个长的开放阅读框(240个氨基酸),推测为转座酶。通过IS3411确定的分子量分别为29000、27000和约10000的三种多肽在微细胞中被鉴定出来。由于Tn3411在整合时产生一个3个碱基对的重复序列,因此将IS3411的核苷酸序列与IS3的核苷酸序列进行了比较。