van Kleef M A, Duine J A
Laboratory of Microbiology and Enzymology, Delft University of Technology, The Netherlands.
Appl Environ Microbiol. 1989 May;55(5):1209-13. doi: 10.1128/aem.55.5.1209-1213.1989.
Quinoprotein content and levels of external pyrroloquinoline quinone (PQQ) were determined for several bacteria under a variety of growth conditions. From these data and those from the literature, a number of factors can be indicated which are relevant for PQQ production. Synthesis of PQQ is only started if synthesis of a quinoprotein occurs, but quinoprotein synthesis does not depend on PQQ synthesis. The presence of quinoprotein substrates is not necessary for quinoprotein and PQQ syntheses. Although the extent of PQQ production was determined by the type of organism and quinoprotein produced, coordination between quinoprotein and PQQ syntheses is loose, since underproduction and overproduction of PQQ with respect to quinoprotein were observed. The results can be interpreted to indicate that quinoprotein synthesis depends on the growth rate whereas PQQ synthesis does not. In that view, the highest PQQ production can be achieved under limiting growth conditions, as was shown indeed by the much higher levels of PQQ produced in fed-batch cultures compared with those produced in batch experiments. The presence of nucleophiles, especially amino acids, in culture media may cause losses of PQQ due to transformation into biologically inactive compounds. Some organisms continued to synthesize PQQ de novo when this cofactor was administered exogenously. Most probably PQQ cannot be taken up by either passive diffusion or active transport mechanisms and is therefore not able to exert feedback regulation on its biosynthesis in these organisms.
测定了多种细菌在不同生长条件下的醌蛋白含量及胞外吡咯喹啉醌(PQQ)水平。根据这些数据以及文献中的数据,可以指出一些与PQQ产生相关的因素。只有当醌蛋白合成发生时,PQQ的合成才会启动,但醌蛋白的合成并不依赖于PQQ的合成。醌蛋白底物的存在对于醌蛋白和PQQ的合成并非必需。尽管PQQ的产生程度由所产生的生物体类型和醌蛋白决定,但醌蛋白与PQQ合成之间的协调是松散的,因为观察到相对于醌蛋白而言,PQQ存在产生不足和过量产生的情况。这些结果可以解释为表明醌蛋白的合成取决于生长速率,而PQQ的合成则不然。从这个角度来看,在限制性生长条件下可以实现最高的PQQ产量,正如补料分批培养中产生的PQQ水平远高于分批实验中产生的PQQ水平所确实表明的那样。培养基中亲核试剂尤其是氨基酸的存在可能会由于转化为生物无活性化合物而导致PQQ的损失。当外源给予这种辅因子时,一些生物体继续从头合成PQQ。很可能PQQ既不能通过被动扩散也不能通过主动转运机制被吸收,因此无法对这些生物体中其生物合成施加反馈调节。