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噬菌体P2的限制性内切酶切割图谱。

A restriction endonuclease cleavage map of bacteriophage P2.

作者信息

Westöö A, Ljungquist E

出版信息

Mol Gen Genet. 1979 Mar 9;171(1):91-102. doi: 10.1007/BF00274019.

Abstract

A restriction endonuclease cleavage map of phage P2 was constructed. The enzymes used and, within parenthesis, the number of their cleavage sites on the P2 lg cc DNA molecule were: AvaI(3), BalI(1), BAMI(3), BglII(3), HaeIII (more than 40; only three were mapped), HindIII(0), HpaI(10), KpnI(3), PstI(3), SalI(2) and SmaI(2). The EcoRI cleavage sites (3), as determined earlier, were used as reference points for this study. The DNAs of a variety of P2 mutants carrying chromosomal aberrations (dell, del2, del3, del6, vir22, vir37(2), vir79 and vir94) were also similarly examined.

摘要

构建了噬菌体P2的限制性内切酶切割图谱。所用的酶以及(括号内为它们在P2 lg cc DNA分子上的切割位点数量):AvaI(3个)、BalI(1个)、BamI(3个)、BglII(3个)、HaeIII(超过40个;仅定位了3个)、HindIII(0个)、HpaI(10个)、KpnI(3个)、PstI(3个)、SalI(2个)和SmaI(2个)。如先前确定的,EcoRI切割位点(3个)用作本研究的参考点。还对携带染色体畸变的多种P2突变体(dell、del2、del3、del6、vir22、vir37(2)、vir79和vir94)的DNA进行了类似检查。

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