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Numbers and locations of native bacteria on field-grown wheat roots quantified by fluorescence in situ hybridization (FISH)

机译:通过荧光原位杂交(FISH)对田间生长的小麦根上的天然细菌数量和位置进行定量

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Native bacteria, Pseudomonas and filamentous bacteria were quantified and localized on wheat roots grown in the field using fluorescence in situ hybridization (FISH). Seminal roots were sampled through the season from unploughed soil in a conservation farming system. Such soils are spatially heterogeneous, and many roots grow slowly through hard soil with cracks and pores containing dead roots remnant from previous crops. Root and rhizosphere morphology, and contact with soil particles were preserved, and autofluorescence was avoided by observing sections in the far-red with Cy5 and Cy5.5 fluorochromes. Spatial analyses showed that bacteria were embedded in a stable matrix (biofilm) within 11 mu m of the root surface (range 2-30 mu m) and were clustered on 40% of roots. Half the clusters colocated with axial grooves between epidermal cells, soil particles, cap cells or root hairs; the other half were not associated with visible features. Across all wheat roots, although variable, bacteria averaged 15.4 x 10(5) cells per mm(3) rhizosphere, and of these, Pseudomonas and filaments comprised 10% and 4%, respectively, with minor effects of sample time, and no effect of plant age. Root caps were most heavily colonized by bacteria along roots, and elongation zones least heavily colonized. Pseudomonas varied little with root development and were 17% of bacteria on the elongation zone. Filamentous bacteria were not found on the elongation zone. The most significant factor to rhizosphere populations along a wheat root, however, was contact with dead root remnants, where Pseudomonas were reduced but filaments increased to 57% of bacteria (P < 0.001). This corresponded with analyses of root remnants showing they were heavily colonized by bacteria, with 48% filaments (P < 0.001) and 1.4%Pseudomonas (P = 0.014). Efforts to manage rhizosphere bacteria for sustainable agricultural systems should continue to focus on root cap and mucilage chemistry, and remnant roots as sources of beneficial bacteria.
机译:使用荧光原位杂交(FISH)对本地细菌,假单胞菌和丝状细菌进行定量,并将其定位在田间生长的小麦根上。在整个季节中,从保护性耕作系统的未耕地土壤中取样精浆根。这样的土壤在空间上是异质的,许多根在坚硬的土壤中缓慢生长,其中的裂缝和气孔含有以前作物残留的死根。保留根和根际形态,并与土壤颗粒接触,并通过用Cy5和Cy5.5荧光染料观察远红部分来避免自发荧光。空间分析表明,细菌被嵌入根表面11微米(范围2-30微米)内的稳定基质(生物膜)中,并聚集在40%的根上。一半的簇与表皮细胞,土壤颗粒,帽细胞或根毛之间的轴向凹槽共存;另一半与可见特征无关。在所有小麦根中,尽管可变,细菌平均每根(3)根际细菌平均有15.4 x 10(5)个细胞,其中假单胞菌和细丝分别占10%和4%,采样时间的影响很小,而没有影响的植物年龄。根冠最容易被细菌沿根部定植,而延伸区最不易被定植。假单胞菌随根的发育变化很小,在延伸区中占细菌的17%。在延伸区未发现丝状细菌。然而,影响小麦根根际根际的最重要因素是与死根残留物接触,假单胞菌减少了,但细丝增加了细菌的57%(P <0.001)。这与对根部残留物的分析相对应,表明根部残留物被细菌大量定殖,其中48%的细丝(P <0.001)和1.4%的假单胞菌(P = 0.014)。为可持续农业系统管理根际细菌的工作应继续集中在根冠和粘液化学上,并将残余根作为有益细菌的来源。

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