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限制酶在流感嗜血杆菌同种或异种转化中不发挥重要作用。

Restriction enzymes do not play a significant role in Haemophilus homospecific or heterospecific transformation.

作者信息

Stuy J H

出版信息

J Bacteriol. 1976 Oct;128(1):212-20. doi: 10.1128/jb.128.1.212-220.1976.

Abstract

Competent Haemophilus influenzae Rd recipients, either as phage HP1 restricting (r+) or nonrestricting (r-) nonlysogens or defective lysogens, were exposed to deoxyribonucleic acids from various wild-type phage HP1 lysogenic H. influenzae serotype strains (non-encapsulated derivatives of serotypes a,b, c, d, and e), to DNA from lysogenic Haemophilus parahaemolyticus, and to DNA from modified and nonmodified phage HP1. Transformation of antibiotic resistance markers and of prophage markers in homospecific crosses was observed to be unaffected by the recipient restriction phenotype, whereas the transfection response was much reduced in r+ recipients. Heterospecific transformation of prophage markers was reduced by only 80 to 90%, whereas antibiotic resistance marker transformation was 1,000 to 10,000 times lower. Heterspecific transfection was at least 100 times lower than homospecific transfection in both r+ and r- recipients. The general conclusion is that neither class I nor class II restriction enzymes affect significantly the transformation efficiency in homospecific and heterospecific crosses. The efficiency of heterospecific transformation may depend mainly on the deoxyribonucleic acid homology in the genetic marker region.

摘要

将有能力的流感嗜血杆菌Rd受体,即作为噬菌体HP1限制型(r+)或非限制型(r-)的非溶原菌或缺陷溶原菌,分别暴露于来自各种野生型噬菌体HP1溶原性流感嗜血杆菌血清型菌株(a、b、c、d和e血清型的非包膜衍生物)的脱氧核糖核酸、来自溶原性副溶血嗜血杆菌的DNA以及来自修饰和未修饰噬菌体HP1的DNA。观察到在同种特异性杂交中,抗生素抗性标记和原噬菌体标记的转化不受受体限制表型的影响,而在r+受体中,转染反应大大降低。原噬菌体标记的异种特异性转化仅降低80%至90%,而抗生素抗性标记转化则低1000至10000倍。在r+和r-受体中,异种特异性转染均比同种特异性转染低至少100倍。总的结论是,I类和II类限制酶均不会显著影响同种特异性和异种特异性杂交中的转化效率。异种特异性转化的效率可能主要取决于遗传标记区域中的脱氧核糖核酸同源性。

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Fate of bacteriophage lambda DNA after adsorption by Haemophilus influenzae.
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A restriction enzyme from Hemophilus influenzae. II.一种来自流感嗜血杆菌的限制性内切酶。II.
J Mol Biol. 1970 Jul 28;51(2):393-409. doi: 10.1016/0022-2836(70)90150-6.

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