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Interactions between the unicellular red alga Rhodella reticulata (Rhodophyta) and contaminated bacteria

机译:单细胞红藻网状红藻(Rhodoella reticulata)与受污染细菌之间的相互作用

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Aims: To define the role of the bacterial strains LR1 and LR3 in the Rhodella cell destruction caused by Cytophaga sp.LR2. Methods and Results: The bacteria were obtained from algal culture with destruction. They were isolated in pure culture and tested for biochemical activities using Polymicrotest. The ability of bacteria to degrade and utilize the algal polysaccharide was investigated. The bacteria were grown in a media containing Rhodella polysaccharide as a sole carbon source. The level of the reducing sugars in the culture media was determined. Scanning electron microscopy (SEM) was used to define the location of bacteria in extensively and intensively cultivated Rhodella reticulata previously infected by Cytophaga sp. LR2. Conclusions: The lysis of Rhodella reticulata cells is due to the joint action of the three bacterial strains with the former pathogen Cytophaga sp. LR2 playing the main role. The accumulation of the polysaccharide and the excreted metabolites of the strains LR1 and LR3 stimulated the development of Cytophaga sp. LR2. The adaptation of the strain to particular conditions of alga cultivation and the utilization of polysaccharide as a sole carbon source supported its stable growth in alga suspension and destruction of Rhodella cells. Significance and Impact of the Study: The predominance of Cytophaga sp. LR2 over the two other contaminantsand the lysis of Rhodella reticulate cells resulted from the ability of the bacterium to attach to the algal polysaccharide sheath. The formation of slime and extrusions facilitated the phenomenon of bacterial adhesion to the algal surface as well as the formation of colonial alga-bacterial spherules. The sedimentation of these aggregates decreased the ability of the algal strain to photosynthesize, led to the lysis of the cells and finally caused the death of Rhodella.
机译:目的:确定LR1和LR3细菌菌株在由食丝菌LR2引起的罗氏杆菌破坏中的作用。方法和结果:细菌是从藻类培养物中获得的,具有破坏性。在纯培养物中分离它们,并使用Polymicrotest测试生化活性。研究了细菌降解和利用藻类多糖的能力。细菌在含有Rhodella多糖作为唯一碳源的培养基中生长。确定培养基中还原糖的水平。扫描电子显微镜(SEM)用于确定细菌在广泛和集约培养的网纹红球菌中的位置,该网纹菌先前已被Cytophaga sp。感染。 LR2。结论:网状红球菌细胞的裂解是由于这三种细菌菌株与原病原菌丝状藻的共同作用。 LR2扮演主要角色。菌株LR1和LR3的多糖和排泄的代谢产物的积累刺激了Cytophaga sp的发育。 LR2。使该菌株适应藻类培养的特定条件,并利用多糖作为唯一碳源,支持其在藻类悬浮液中的稳定生长和对红球菌细胞的破坏。研究的意义和影响:Cytophaga sp。的优势。 LR2在另外两种污染物上的溶解以及罗德氏菌网状细胞的裂解是由于细菌附着于藻类多糖鞘的能力所致。粘液和挤压物的形成促进了细菌粘附到藻类表面的现象以及殖民地藻类细菌小球的形成。这些聚集体的沉淀降低了藻株光合作用的能力,导致细胞裂解,并最终导致罗得氏菌死亡。

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