Baldwin W W, Kirkish M A, Koch A L
Indiana University School of Medicine, Northwest Center for Medical Education, Gary 46408.
J Bacteriol. 1994 Aug;176(16):5001-4. doi: 10.1128/jb.176.16.5001-5004.1994.
The growth rates and buoyant densities of a Salmonella typhimurium mutant, TL126 (proB74A+), with enhanced osmotolerance caused by proline overproduction were measured and compared with the growth rates and buoyant densities of an isogenic (wild-type) strain, TL128 (proB+ A+), with normal control of proline production. Growth rates were determined in a rich medium (Luria broth) with added NaCl to produce various osmotic strengths ranging from 300 to 2,000 mosM. At low concentrations of NaCl, there was little variation in doubling times between the two strains. However, as the osmotic strength of the medium approached and exceeded 1,300 mosM, the doubling times of TL126 (osmotolerant) were 1.5 to 2 times faster than those of TL128 (wild type), confirming the osmotolerance of TL126. Buoyant densities were determined by equilibrium sedimentation in a Percoll gradient of osmotic strength equal to that of the growth medium. The osmolarity of the Percoll gradient was adjusted by the addition of NaCl. At low osmolarities (300 to 500 mosM), the buoyant density of TL126 (osmotolerant) was slightly but consistently lower than that of TL128 (wild type). As the osmotic strength was increased, the buoyant density of TL126 (osmotolerant) increased in proportion to the osmotic strength. In contrast, the buoyant density of strain TL128 (wild type) did not increase as much. At high osmolarities (1,600 to 2,000 mosM), the buoyant density of TL126 (osmotolerant) was consistently higher than that of TL128 (wild type). These results suggest that the intracellular accumulation of proline by TL126, the osmotolerant strain, increases both the growth rates and buoyant densities at osmolarities of 1,300 mosM and above.
测定了一株因脯氨酸过量产生而具有增强渗透压耐受性的鼠伤寒沙门氏菌突变体TL126(proB74A+)的生长速率和浮力密度,并将其与脯氨酸产生受到正常调控的同基因(野生型)菌株TL128(proB+ A+)的生长速率和浮力密度进行了比较。在添加了NaCl的丰富培养基(Luria肉汤)中测定生长速率,以产生从300到2000 mosM的各种渗透压强度。在低浓度NaCl下,两株菌的倍增时间几乎没有差异。然而,随着培养基的渗透压强度接近并超过1300 mosM,TL126(渗透压耐受性菌株)的倍增时间比TL128(野生型)快1.5至2倍,证实了TL126的渗透压耐受性。通过在渗透强度与生长培养基相等的Percoll梯度中进行平衡沉降来测定浮力密度。通过添加NaCl来调节Percoll梯度的渗透压。在低渗透压(300至500 mosM)下,TL126(渗透压耐受性菌株)的浮力密度略低于但始终低于TL128(野生型)。随着渗透压强度增加,TL126(渗透压耐受性菌株)的浮力密度与渗透压强度成比例增加。相比之下,菌株TL128(野生型)的浮力密度增加幅度没有那么大。在高渗透压(1600至2000 mosM)下,TL126(渗透压耐受性菌株)的浮力密度始终高于TL128(野生型)。这些结果表明,渗透压耐受性菌株TL126细胞内脯氨酸的积累在渗透压为1300 mosM及以上时,会同时提高生长速率和浮力密度。