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首页> 外文期刊>Soil Biology & Biochemistry >Identification of microbial communities that assimilate substrate from root cap cells in an aerobic soil using a DNA-SIP approach
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Identification of microbial communities that assimilate substrate from root cap cells in an aerobic soil using a DNA-SIP approach

机译:使用DNA-SIP方法鉴定需氧土壤中根冠细胞吸收底物的微生物群落

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Although root cap cells are an important substrate for microorganisms in the rhizosphere, little attention has been paid to the decomposition of sloughed root cap cells by microorganisms. This study used rice plant callus cells grown on medium containing C-13-labelled glucose as a model material for rice plant root cap cells. Harvested C-13-labelled callus cells (78 atom % C-13) were subjected to decomposition in an aerobic soil microcosm for 56 days. The low cellulose and lignin levels and the disaggregated nature of the callus cells indicated that these cells were an appropriate model material for root cap cells. DNA was extracted from a soil incubated with C-12- and C-13-callus cells and subjected to buoyant density gradient centrifugation to identify bacterial species that assimilated carbon from the callus cells. The stability of the total bacterial communities during the incubation was estimated. Many DGGE bands in light fractions of soil incubated with C-13-callus cells were weaker in intensity than those from soil incubated with C-12-callus cells, and those bands were shifted to heavier fractions after C-13-callus treatment. C-13-labelled DNA was detected from Day 3 onwards, and the DGGE bands in the heavy fractions were most numerous on Day 21. DGGE bands from heavy and light fractions were sequenced, revealing more than 70% of callus- C incorporating bacteria were Gram-negative, predominantly alpha-Proteobacteria, beta-Proteobacteria, gamma-Proteobacteria, Sphingobacteria and Actinobacteria. These species were phylogenetically distinct from the bacteria reported to be present during plant residue decomposition and resident in rice roots. This study indicates that root cap cells are decomposed by specific bacterial species in the rhizosphere, and that these species augment the diversity of rhizospheric bacterial communities
机译:尽管根冠细胞是根际中微生物的重要底物,但很少有人关注微生物对腐烂的根冠细胞的分解。这项研究使用生长在含有C-13标记葡萄糖的培养基上的水稻愈伤组织细胞作为水稻根冠细胞的模型材料。将收获的C-13标记的愈伤组织细胞(78原子%的C-13)在需氧土壤微观世界中分解56天。低纤维素和木质素水平以及愈伤组织细胞的分解性质表明,这些细胞是根冠细胞的合适模型材料。从与C-12和C-13愈伤组织细胞孵育的土壤中提取DNA,并进行浮力密度梯度离心,以鉴定从愈伤组织细胞吸收碳的细菌种类。估计在孵育过程中总细菌群落的稳定性。 C-13愈伤组织细胞孵育的土壤轻质部分中的许多DGGE谱带的强度比C-12愈伤组织细胞孵育的土壤中的DGGE强度弱,在C-13愈伤组织处理后,这些DGGE谱带转移至较重的部分。从第3天开始检测到C-13标记的DNA,重馏分中的DGGE条带在第21天最多。对重馏分和轻馏分的DGGE条带进行了测序,结果发现超过70%的愈伤组织C掺入了细菌革兰氏阴性,主要是α-Proteobacteria,β-Proteobacteria,γ-Proteobacteria,Sphingobacteria和Actinobacteria。这些物种在系统发育上不同于据报道在植物残渣分解过程中存在并存在于稻根中的细菌。这项研究表明根冠细胞被根际中的特定细菌物种分解,并且这些物种增加了根际细菌群落的多样性

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