Liu J K, Lu M W, Yang L T, Lin C S
Department of Biology, National Sun Yat-sen University, Taiwan, ROC.
Proc Natl Sci Counc Repub China B. 1996 Oct;20(4):110-6.
This paper examines the effects of phosphate pool and expression of polyphosphate kinase on glucose uptake by expressing the polyphosphate kinase under the control of lac promoter. The E. coli transformant of pL1, containing an IPTG controllable element for polyphosphate kinase expression, showed that the total intracellular phosphate significantly increased. However, the rate of glucose uptake by the resting plasmid-bearing cells with IPTG induction significantly decreased. These findings suggest that the polyphosphate can not directly function as an energy source in E. coli or at least not as a good energy supplier.
本文通过在乳糖启动子控制下表达多聚磷酸激酶,研究了磷酸池和多聚磷酸激酶表达对葡萄糖摄取的影响。含有用于多聚磷酸激酶表达的IPTG可控元件的pL1大肠杆菌转化体表明,细胞内总磷酸盐显著增加。然而,经IPTG诱导的携带质粒的静止细胞对葡萄糖的摄取速率显著降低。这些发现表明,多聚磷酸盐不能直接在大肠杆菌中作为能量来源发挥作用,或者至少不是一个良好的能量供应者。