PURIFICATION, CRYSTALLIZATION AND PRELIMINARY-X-RAY DIFFRACTION STUDIES OF THE PVUII-ENDONUCLEASE

被引:7
作者
ATHANASIADIS, A [1 ]
KOKKINIDIS, M [1 ]
机构
[1] UNIV CRETE,INST MOLEC BIOL & BIOTECHNOL,GR-71110 HERAKLION,GREECE
关键词
RESTRICTION-MODIFICATION SYSTEMS; PVUII-ENDONUCLEASE; ENZYME PURIFICATION; PROTEIN CRYSTALLIZATION; HANGING-DROP TECHNIQUE;
D O I
10.1016/0022-2836(91)90486-P
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The PvuII endonuclease (PvuIIR) is a restriction enzyme from a type II restriction-modification system of Proteus vulgaris coded on plasmid pPvul. The protein recognizes the DNA sequence 5′ CAG'CTG 3′ and shows no sequence homology to other restriction enzymes. This makes PvuIIR an interesting subject for structural determination. A purification procedure was developed that yields milligram quantities of the PvuIIR from plasmids expressed in the Escherichia coli strain HB101. The protein was crystallized using ammonium sulphate as precipitant. The crystals are orthorhombic, space group P21212 with cell dimensions: a = 84·2 A ̊, b = 106·2 A ̊, c = 46·9 A ̊. The asymmetric unit contains one PvuIIR dimer. Diffraction extends to 2·3 Å, so the crystals may permit structural determination at atomic resolution. © 1991.
引用
收藏
页码:451 / 453
页数:3
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