Katz L, Englesberg E
J Bacteriol. 1971 Jul;107(1):34-52. doi: 10.1128/jb.107.1.34-52.1971.
Mutations in gene araB producing an l-arabinose-negative phenotype cause either an increase (hyperinducible), decrease (polar), or have no effect at all on the inducible rate of expression of the l-arabinose operon. Fourteen araB gene mutants exhibiting such effects were shown to be the result of: nonsense, frameshift, or missense mutations. All missense mutants were hyperinducible, exhibiting approximately a twofold increase in rate of l-arabinose isomerase production. All frameshift and most nonsense mutants exhibited polar effect. One nonsense mutant was hyperinducible. The cis-dominant polar effect of nonsense and frameshift mutants (as compared to induced wild type) were more pronounced in arabinose-utilizing merodiploids and in araBaraC(c) double mutants where inducible and constitutive enzyme levels are respectively determined. On the other hand, in arabinose-utilizing merodiploids, missense mutations no longer exhibited hyperinducibility but displayed a wild-type level of operon expression. Increases in the wild type-inducible rate of expression of the operon were found when growth rate was dependent on the concentration of l-arabinose. Cyclic 3',5'-adenosine monophosphate also stimulated expression of the operon with the wild type in a mineral l-arabinose medium. These observations are explained on the basis that the steady-state expression of the l-arabinose operon OIBAD is dependent on the concentration of (i) l-arabinose, the effector of this system, which stimulates the expression of the operon, and (ii) catabolite repressors, produced from l-arabinose, which dampen the expression of the operon. We have termed the latter phenomenon "self-catabolite" repression.
产生L-阿拉伯糖阴性表型的araB基因突变对L-阿拉伯糖操纵子的诱导表达速率会造成增加(超诱导)、降低(极性效应)或根本没有影响。十四种表现出此类效应的araB基因突变体被证明是由以下原因导致的:无义突变、移码突变或错义突变。所有错义突变体都是超诱导型的,L-阿拉伯糖异构酶的产生速率增加了约两倍。所有移码突变体和大多数无义突变体都表现出极性效应。一个无义突变体是超诱导型的。无义突变体和移码突变体的顺式显性极性效应(与诱导的野生型相比)在利用阿拉伯糖的部分二倍体以及araBaraC(c)双突变体中更为明显,在这些突变体中可分别测定诱导型和组成型酶水平。另一方面,在利用阿拉伯糖的部分二倍体中,错义突变不再表现出超诱导性,而是呈现出野生型水平的操纵子表达。当生长速率取决于L-阿拉伯糖的浓度时,发现操纵子的野生型诱导表达速率会增加。在无机L-阿拉伯糖培养基中,环3',5'-腺苷单磷酸也能刺激野生型操纵子的表达。基于以下原因对这些观察结果进行了解释:L-阿拉伯糖操纵子OIBAD的稳态表达取决于(i)L-阿拉伯糖的浓度,L-阿拉伯糖是该系统的效应物,可刺激操纵子的表达;(ii)由L-阿拉伯糖产生的分解代谢物阻遏物,它会抑制操纵子的表达。我们将后一种现象称为“自身分解代谢物”阻遏。