Keller J A, Simon L D
J Bacteriol. 1987 Apr;169(4):1585-92. doi: 10.1128/jb.169.4.1585-1592.1987.
Escherichia coli mutants were isolated that supported the growth of a lambda Ots and, in at least one case, a lambda Bts phage at the normally nonpermissive temperature of 39 degrees C. In one such strain, Ots and Bts suppression ability appeared to be a function of the guaB gene. Ots suppression by the mutant guaB strain was prevented if high levels of guanine or xanthine were present in the medium. No other base had any effect on Ots suppression in this strain. Other strains carrying spontaneous mutations resulting in guanine or xanthine auxotrophy (guaA or guaB lesions, respectively) all allowed lambda Ots replication at 39 degrees C; Ots suppression in these strains was also abolished by addition of guanine to the medium. Thus, reduced intracellular guanine levels resulting from guaA or guaB mutations appeared to suppress the inability of lambda Ots and, at least in some cases, Bts bacteriophage to form plaques at 39 degrees C. In burst size experiments, a guaB mutant produced a larger phage yield per infected cell of both lambda Ots and lambda O+ phage at 39 degrees C than did a similar guaB+ strain. It appeared that a lower-than-normal level of guanine (or a guanine derivative) in these cells may permit unusually efficient lambda replication. The fact that O+ and lambda Ots bursts in the guaB mutant were reduced significantly by addition of exogenous guanine to the medium is consistent with this suggestion. Another strain that suppresses the Ots allele has no known auxotrophic requirements, and suppression in this strain was unaffected by addition of guanine to the medium; however, addition of cytidine to the medium specifically eliminated Ots suppression in this strain. The mutation responsible for allowing Ots replication in this strain is unknown.
分离出了大肠杆菌突变体,这些突变体能够支持λOts噬菌体生长,并且在至少一个案例中,还能支持λBts噬菌体在39℃这一通常非允许温度下生长。在其中一个这样的菌株中,Ots和Bts抑制能力似乎是guaB基因的一种功能。如果培养基中存在高水平的鸟嘌呤或黄嘌呤,突变的guaB菌株对Ots的抑制作用就会被阻止。在该菌株中,其他碱基对Ots抑制没有任何影响。携带导致鸟嘌呤或黄嘌呤营养缺陷型(分别为guaA或guaB损伤)的自发突变的其他菌株,都能使λOts在39℃下复制;向这些菌株的培养基中添加鸟嘌呤也会消除Ots抑制作用。因此,由guaA或guaB突变导致的细胞内鸟嘌呤水平降低,似乎抑制了λOts以及至少在某些情况下λBts噬菌体在39℃下形成噬菌斑的无能。在爆发量实验中,一个guaB突变体在39℃下每感染细胞产生的λOts和λO+噬菌体产量,比类似的guaB+菌株更高。似乎这些细胞中低于正常水平的鸟嘌呤(或鸟嘌呤衍生物)可能允许异常高效的λ复制。向培养基中添加外源鸟嘌呤会显著降低guaB突变体中O+和λOts的爆发量,这一事实与该推测一致。另一个抑制Ots等位基因的菌株没有已知的营养缺陷需求,并且该菌株中的抑制作用不受向培养基中添加鸟嘌呤的影响;然而,向培养基中添加胞苷会特异性消除该菌株中的Ots抑制作用。导致该菌株中Ots复制的突变尚不清楚。