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        Isolation and Characterization of Plant Growth-Promoting Rhizobacteria from Wheat Roots by Wheat Germ Agglutinin Labeled with Fluorescein Isothiocyanate

        Jian Zhang,Jingyang Liu,Liyuan Meng,Zhongyou Ma,Xinyun Tang,Yuanyuan Cao,Leni Sun 한국미생물학회 2012 The journal of microbiology Vol.50 No.2

        Thirty-two isolates were obtained from wheat rhizosphere by wheat germ agglutinin (WGA) labeled with fluorescein isothiocyanate (FITC). Most isolates were able to produce indole acetic acid (65.6%) and siderophores (59.3%), as well as exhibited phosphate solubilization (96.8%). Fourteen isolates displayed three plant growth-promoting traits. Among these strains, two phosphate-dissolving ones, WS29 and WS31, were evaluated for their beneficial effects on the early growth of wheat (Triticum aestivum Wan33). Strain WS29and WS31 significantly promoted the development of lateral roots by 34.9% and 27.6%, as well as increased the root dry weight by 25.0% and 25.6%, respectively, compared to those of the control. Based on 16S rRNA gene sequence comparisons and phylogenetic positions, both isolates were determined to belong to the genus Bacillus. The proportion of isolates showing the properties of plant growth-promoting rhizobacteria (PGPR) was higher than in previous reports. The efficiency of the isolation of PGPR strains was also greatly increased by WGA labeled with FITC. The present study indicated that WGA could be used as an effective tool for isolating PGPR strains with high affinity to host plants from wheat roots. The proposed approach could facilitate research on biofertilizers or biocontrol agents.

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        The Role of Wheat Germ Agglutinin in the Attachment of Pseudomonas sp. WS32 to Wheat Root

        Jian Zhang,Liyuan Meng,Yuanyuan Cao,Huiping Chang,Zhongyou Ma,Leni Sun,Ming Zhang,Xinyun Tang 한국미생물학회 2014 The journal of microbiology Vol.52 No.12

        Wheat germ agglutinin (WGA), which is secreted on thesurface of wheat root, has been defined as a protein that reversiblyand non-enzymatically binds to specific carbohydrates. However, little attention has been paid to the functionof WGA in the attachment of bacteria to their host plants. The aim of this study was to investigate the role of WGA inthe attachment of Pseudomonas sp. WS32 to wheat roots. Wheat roots were initially treated with double-distilled water,WGA-H (WGA solution that was heated at 100°C for 15 min)and WGA, independently. Subsequently, the roots were coincubatedwith cell solutions (109 cells/ml). A dilution platemethod using a solid nutrient medium was employed to determinethe adsorption of WS32 to wheat roots. WGA waslabeled with fluorescein isothiocyanate and detected usingthe fluorescent in situ hybridization (FISH) technique. Thenumber of adsorptive WS32 cells on wheat roots was significantlyincreased when the wheat roots were pretreatedwith WGA, compared with the control treatment (p = 0.01). However, WGA-H failed to increase the amount of bacterialcells that attached to the wheat roots because of the lossof its physiological activity. The FISH assay also revealedthat more cells adhered to WGA-treated wheat roots than tocontrol or WGA-H-treated roots. The results indicated thatWGA can mediate Pseudomonas strain WS32’s adherenceto wheat seedling roots. The findings of this study provide abetter understanding of the processes involved in plant-microbe interactions.

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