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利用 pqqE 基因作为与植物相关的革兰氏阴性解磷菌溯源的分子标记。

Employment of pqqE gene as molecular marker for the traceability of Gram negative phosphate solubilizing bacteria associated to plants.

机构信息

Instituto de Investigaciones Agrobiotecnológicas (CONICET-UNRC), Río Cuarto, Argentina.

Instituto de Microbiología y Zoología Agrícola, IMyZA, IABiMo, INTA, Hurlingham, Buenos Aires, Argentina.

出版信息

Curr Genet. 2024 Aug 2;70(1):12. doi: 10.1007/s00294-024-01296-4.

Abstract

Insoluble phosphorous compounds solubilization by soil bacteria is of great relevance since it puts available the phosphorus to be used by plants. The production of organic acids is the main microbiological mechanism by which insoluble inorganic phosphorus compounds are solubilized. In Gram negative bacteria, gluconic acid is synthesized by the activity of the holoenzyme glucose dehydrogenase-pyrroloquinoline quinine named GDH-PQQ. The use of marker genes is a very useful tool to evaluate the persistence of the introduced bacteria and allow to follow-up the effect of biotic and abiotic factors on these beneficial microorganisms in the soil. In previous studies we detected the presence of the pqqE gene in a great percentage of both non-culturable and culturable native soil bacteria. The objective of this study was to analyze the phylogeny of the sequence of pqqE gene and its potential for the study of phosphate solubilizing bacteria from pure and mixed bacterial cultures and rhizospheric soil samples. For this, the presence of the pqqE gene in the genome of phosphate solubilizing bacteria that belong to several bacteria was determined by PCR. Also, this gene was analyzed from mixed bacterial cultures and rhizospheric soil associated to peanut plants inoculated or not with phosphate solubilizing bacteria. For this, degenerate primers designed from several bacterial genera and specific primers for the genus Pseudomonas spp., designed in this study, were used. DNA template used from simple or mixed bacterial cultures and from rhizospheric soil samples was obtained using two different DNA extraction techniques. Results indicated that pqqE gene amplification product was found in the genome of all Gram negative phosphate solubilizing bacteria analyzed. It was possible to detect this gene in the DNA obtained from mixed cultures where these bacteria grew in interaction with other microorganisms and in that obtained from rhizospheric soil samples inoculated or not with these bacteria. The phylogenetic analysis indicated that pqqE gene is a conserved gene within related genera. In conclusion, pqqE gene could be a potential marker for the study of phosphate solubilizing bacterial populations.

摘要

土壤细菌对不溶性磷化合物的溶解具有重要意义,因为它使植物可用的磷得以释放。有机酸的产生是微生物溶解不溶性无机磷化合物的主要机制。在革兰氏阴性菌中,葡萄糖脱氢酶-吡咯喹啉醌(GDH-PQQ)全酶活性合成葡萄糖酸。标记基因的使用是评估引入细菌持久性的非常有用的工具,并允许跟踪生物和非生物因素对土壤中这些有益微生物的影响。在之前的研究中,我们在大量非可培养和可培养的本土土壤细菌中检测到 pqqE 基因的存在。本研究的目的是分析 pqqE 基因序列的系统发育及其在纯和混合细菌培养物和根际土壤样品中溶磷细菌研究中的潜力。为此,通过 PCR 确定属于几个细菌的溶磷细菌基因组中 pqqE 基因的存在。此外,还从混合细菌培养物和与花生植物接种或不接种溶磷细菌相关的根际土壤中分析了该基因。为此,使用了从几个细菌属设计的简并引物和本研究中设计的用于假单胞菌属的特异性引物。从简单或混合细菌培养物和根际土壤样品中获得的 DNA 模板使用两种不同的 DNA 提取技术获得。结果表明,在分析的所有革兰氏阴性溶磷细菌的基因组中都发现了 pqqE 基因扩增产物。可以在这些细菌与其他微生物相互作用生长的混合培养物中以及在接种或不接种这些细菌的根际土壤样品中获得的 DNA 中检测到该基因。系统发育分析表明,pqqE 基因是相关属内保守的基因。总之,pqqE 基因可能是研究溶磷细菌种群的潜在标记。

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