Shamanna D K, Sanderson K E
J Bacteriol. 1979 Jul;139(1):64-70. doi: 10.1128/jb.139.1.64-70.1979.
Salmonella typhimurium LT2 grows on D-xylose as sole carbon source with a generation time of 105 to 110 min. The following activities are induced at the indicated time after the addition of the inducer, D-xylose: D-xylulokinase (5 min), D-xylose isomerase (7 to 8 min), and D-xylose transport (10 min). All other pentoses and pentitols tested failed to induce isomerase or kinase. Synthesis of D-xylose isomerase was subject to catabolite repression, which was reversed by the addition of cyclic adenosine monophosphate. Most of the radioactive counts from D-[14C]xylose were initially accumulated in the cell in the form of D-xylose or D-xylulose. D-Xylose uptake in a mutant which was deficient in D-xylose isomerase was equal to that of the wild type. The apparent Km for D-xylose uptake was 0.41 mM. Some L-arabinose was accumulated in D-xylose-induced cells, and some D-xylose was accumulated in L-arabinose-induced cells. D-Xylitol and L-arabinose competed against C-xylose uptake, but D-arabinose, D-lyxose, and L-lyxose did not. Osmotic shock reduced the uptake of D-xylose by about 50%; by equilibrium dialysis, a D-xylose-binding protein was detected in the supernatant fluid after spheroplasts were formed from D-xylose-induced cells.
鼠伤寒沙门氏菌LT2能以D-木糖作为唯一碳源生长,其代时为105至110分钟。在添加诱导剂D-木糖后的指定时间诱导出以下活性:D-木酮糖激酶(5分钟)、D-木糖异构酶(7至8分钟)和D-木糖转运(10分钟)。所测试的所有其他戊糖和戊糖醇均未能诱导异构酶或激酶。D-木糖异构酶的合成受分解代谢物阻遏,添加环磷酸腺苷可逆转这种阻遏。D-[14C]木糖的大部分放射性计数最初以D-木糖或D-木酮糖的形式在细胞中积累。在缺乏D-木糖异构酶的突变体中,D-木糖的摄取与野生型相同。D-木糖摄取的表观Km为0.41 mM。在D-木糖诱导的细胞中积累了一些L-阿拉伯糖,在L-阿拉伯糖诱导的细胞中积累了一些D-木糖。D-木糖醇和L-阿拉伯糖与C-木糖摄取竞争,但D-阿拉伯糖、D-来苏糖和L-来苏糖则不然。渗透休克使D-木糖的摄取减少约50%;通过平衡透析,在由D-木糖诱导的细胞形成原生质球后,在上清液中检测到一种D-木糖结合蛋白。