Parche Stephan, Beleut Manfred, Rezzonico Enea, Jacobs Doris, Arigoni Fabrizio, Titgemeyer Fritz, Jankovic Ivana
Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland.
J Bacteriol. 2006 Feb;188(4):1260-5. doi: 10.1128/JB.188.4.1260-1265.2006.
Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP. The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals.
对长双歧杆菌NCC2705在葡萄糖和乳糖上生长所获得的培养上清液进行分析发现,在乳糖耗尽之前,葡萄糖的利用受到损害。因此,与许多其他细菌不同,长双歧杆菌优先利用乳糖而非葡萄糖作为主要碳源。对长双歧杆菌细胞进行的葡萄糖摄取实验表明,在乳糖存在的情况下,葡萄糖转运受到抑制。使用DNA阵列对全局基因表达谱进行比较分析,结果仅鉴定出一个受乳糖抑制的基因,即假定的葡萄糖转运蛋白基因glcP。通过对葡萄糖转运缺陷型大肠杆菌菌株进行异源互补,证明了GlcP作为葡萄糖转运蛋白的功能。此外,GlcP对葡萄糖表现出最高的底物特异性。引物延伸和实时PCR分析证实,glcP的表达由乳糖介导。因此,我们的数据表明,培养基中乳糖的存在导致葡萄糖转运受到抑制以及葡萄糖转运蛋白基因glcP的转录下调。这可能反映了长双歧杆菌在哺乳动物胃肠道中高度适应的生活方式。