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首页> 外文期刊>Applied Microbiology >Regulation of Pyrroloquinoline Quinone-Dependent Glucose Dehydrogenase Activity in the Model Rhizosphere-Dwelling Bacterium Pseudomonas putida KT2440
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Regulation of Pyrroloquinoline Quinone-Dependent Glucose Dehydrogenase Activity in the Model Rhizosphere-Dwelling Bacterium Pseudomonas putida KT2440

机译:吡咯喹啉醌依赖性葡萄糖脱氢酶活性在模型根际居住细菌假单胞菌恶臭假单胞菌KT2440中的调节

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Soil-dwelling microbes solubilize mineral phosphates by secreting gluconic acid, which is produced from glucose by a periplasmic glucose dehydrogenase (GDH) that requires pyrroloquinoline quinone (PQQ) as a redox coenzyme. While GDH-dependent phosphate solubilization has been observed in numerous bacteria, little is known concerning the mechanism by which this process is regulated. Here we use the model rhizosphere-dwelling bacterium Pseudomonas putida KT2440 to explore GDH activity and PQQ synthesis, as well as gene expression of the GDH-encoding gene ( gcd ) and PQQ biosynthesis genes ( pqq operon) while under different growth conditions. We also use reverse transcription-PCR to identify transcripts from the pqq operon to more accurately map the operon structure. GDH specific activity and PQQ levels vary according to growth condition, with the highest levels of both occurring when glucose is used as the sole carbon source and under conditions of low soluble phosphate. Under these conditions, however, PQQ levels limit in vitro phosphate solubilization. GDH specific activity data correlate well with gcd gene expression data, and the levels of expression of the pqqF and pqqB genes mirror the levels of PQQ synthesized, suggesting that one or both of these genes may serve to modulate PQQ levels according to the growth conditions. The pqq gene cluster ( pqqFABCDEG ) encodes at least two independent transcripts, and expression of the pqqF gene appears to be under the control of an independent promoter and terminator.IMPORTANCE Plant growth promotion can be enhanced by soil- and rhizosphere-dwelling bacteria by a number of different methods. One method is by promoting nutrient acquisition from soil. Phosphorus is an essential nutrient that plants obtain through soil, but in many cases it is locked up in forms that are not available for plant uptake. Bacteria such as the model bacterium Pseudomonas putida KT2440 can solubilize insoluble soil phosphates by secreting gluconic acid. This chemical is produced from glucose by the activity of the bacterial enzyme glucose dehydrogenase, which requires a coenzyme called PQQ. Here we have studied how the glucose dehydrogenase enzyme and the PQQ coenzyme are regulated according to differences in bacterial growth conditions. We determined that glucose dehydrogenase activity and PQQ production are optimal under conditions when the bacterium is grown with glucose as the sole carbon source and under conditions of low soluble phosphate.
机译:居住在土壤中的微生物通过分泌葡萄糖酸来溶解无机磷酸盐,葡萄糖酸是由需要吡咯并喹啉醌(PQQ)作为氧化还原辅酶的周质葡萄糖脱氢酶(GDH)从葡萄糖中产生的。尽管已在许多细菌中观察到了依赖GDH的磷酸盐增溶作用,但对于调节该过程的机理知之甚少。在这里,我们使用模型根际居住细菌恶臭假单胞菌KT2440探索GDH活性和PQQ合成,以及在不同生长条件下GDH编码基因(gcd)和PQQ生物合成基因(pqq操纵子)的基因表达。我们还使用逆转录PCR从pqq操纵子中识别转录本,以更准确地定位操纵子结构。 GDH的比活和PQQ的水平根据生长条件而变化,当葡萄糖用作唯一的碳源时和在低可溶性磷酸盐的条件下,两者的含量最高。但是,在这些条件下,PQQ的水平限制了体外磷酸盐的溶解。 GDH比活性数据与gcd基因表达数据很好地相关,并且pqqF和pqqB基因的表达水平反映了合成的PQQ的水平,表明这些基因中的一个或两个都可以根据生长条件来调节PQQ的水平。 pqq基因簇(pqqFABCDEG)至少编码两个独立的转录本,并且pqqF基因的表达似乎受独立的启动子和终止子的控制。重要的是,土壤和根际土壤中的细菌可以通过促进植物生长来促进许多不同的方法。一种方法是促进从土壤中获取养分。磷是植物通过土壤获得的必需营养素,但在许多情况下,磷被锁定为植物无法吸收的形式。细菌,例如模型细菌恶臭假单胞菌KT2440可以通过分泌葡萄糖酸来溶解不溶性土壤磷酸盐。这种化学物质是由葡萄糖通过细菌酶葡萄糖脱氢酶的活性产生的,该酶需要一种称为PQQ的辅酶。在这里,我们研究了如何根据细菌生长条件的差异来调节葡萄糖脱氢酶和PQQ辅酶。我们确定,在细菌以葡萄糖作为唯一碳源生长的条件下和低可溶性磷酸盐条件下,葡萄糖脱氢酶活性和PQQ产量最佳。

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