Rick P D, Young D A
J Bacteriol. 1982 May;150(2):456-64. doi: 10.1128/jb.150.2.456-464.1982.
The relationship between the inability to synthesize a complete 3-deoxy-D-manno-octulosonate region of lipopolysaccharide and cell death was investigated in a temperature-sensitive lethal mutant of Salmonella typhimurium. The defect in lipopolysaccharide synthesis is due to a mutation in the structural gene for 3-deoxy-D-manno-octulosonate-8-phosphate synthetase (designated kdsA) and results in the synthesis of a temperature-sensitive enzyme. Expression of the kdsA lesion at elevated temperatures, at which the synthesis of 3-deoxy-D-manno-octulosonate is complete blocked, is required for expression of the temperature-sensitive lethal phenotype. However, the defect in lipopolysaccharide synthesis is not alone sufficient cause for the observed cell death. Genetic evidence if presented which indicates that the mutant possesses a second mutation, or possibly multiple mutations, whose lethal expression is dependent on the inability of the mutant to synthesize a fully acylated and 3-deoxy-D-manno-octulosonate-substituted lipid A portion of lipopolysaccharide at elevated temperatures.
在鼠伤寒沙门氏菌的一个温度敏感致死突变体中,研究了脂多糖完整3-脱氧-D-甘露糖辛酮酸区域合成能力缺失与细胞死亡之间的关系。脂多糖合成缺陷是由于3-脱氧-D-甘露糖辛酮酸-8-磷酸合成酶(命名为kdsA)的结构基因突变所致,导致合成一种温度敏感型酶。在高温下kdsA损伤的表达,此时3-脱氧-D-甘露糖辛酮酸的合成被完全阻断,是温度敏感致死表型表达所必需的。然而,脂多糖合成缺陷并非观察到的细胞死亡的唯一充分原因。所提供的遗传学证据表明,该突变体具有第二个突变,或可能多个突变,其致死表达取决于该突变体在高温下无法合成完全酰化且3-脱氧-D-甘露糖辛酮酸取代的脂多糖脂质A部分。