Caster J H, Goodgal S H
Department of Microbiology, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
J Bacteriol. 1972 Oct;112(1):492-502. doi: 10.1128/jb.112.1.492-502.1972.
In studies of competence-deficient mutants of Haemophilus influenzae which absorb deoxyribonucleic acid (DNA) but fail to produce transformants, it was observed that in some mutants the residual transforming activity for different markers varied widely, i.e., produced a ratio effect. One of these mutants, com(-56), was studied intensively to determine the cause of the residual efficiency of transformation and the reason for the ratio effect. The residual frequency of transformation was higher for markers considered single-site mutations (like naladixic acid resistance), whereas the least efficient markers tested were those conferring resistance to high levels of streptomycin or novobiocin which are more complex than single-site mutations. Measurement of frequencies of cotransformation indicated that overall genetic linkage was reduced. Transfection was fairly efficient with phage S2 DNA, but not prophage DNA. Donor marker activity could be detected in transformed cell lysates, but not linked to recipient markers in recombinant molecules. Sucrose gradient analysis of such lysates revealed that donor material was associated with recipient DNA in at least normal quantities, but lacked detectable genetic activity. Material from donor DNA labeled with heavy isotopes was incorporated into recipient chromosomal fragments having a density indistinguishable from normal density, unlike the hybrid density recombinant material found in normal cells. No excessive solubilization or nicking of unincorporated donor was detected. It is postulated that this strain contains a hyperactive nuclease, which reduces the effective size of the input DNA during the integration process.
在对流感嗜血杆菌能力缺陷型突变体的研究中,这些突变体能够吸收脱氧核糖核酸(DNA)但无法产生转化体,研究发现,在一些突变体中,不同标记的残余转化活性差异很大,即产生了比率效应。其中一个突变体com(-56)被深入研究,以确定转化残余效率的原因和比率效应的原因。对于被认为是单位点突变的标记(如萘啶酸抗性),转化的残余频率较高,而测试的效率最低的标记是那些赋予对高水平链霉素或新生霉素抗性的标记,这些抗性比单位点突变更复杂。共转化频率的测量表明总体遗传连锁减少。用噬菌体S2 DNA进行转染相当有效,但用原噬菌体DNA则无效。在转化细胞裂解物中可以检测到供体标记活性,但在重组分子中与受体标记没有联系。对此类裂解物的蔗糖梯度分析表明,供体物质与受体DNA至少以正常数量相关联,但缺乏可检测到的遗传活性。用重同位素标记的供体DNA的物质被整合到密度与正常密度无法区分的受体染色体片段中,这与正常细胞中发现的杂种密度重组物质不同。未检测到未整合供体的过度溶解或切口。据推测,该菌株含有一种超活性核酸酶,它在整合过程中会减小输入DNA的有效大小。