高产水稻土细菌多样性的培养法与非培养法比较研究

利用细菌的通用引物扩增江西余江县高产水稻土红壤细菌总DNA和平板培养细菌混合总DNA的16S rDNA基因片段,在此基础上分别建立两种16S rDNA文库(文库a和文库b)。从两个文库中各随机挑选100个克隆,扩增出阳性克隆中的插入片段后选用HhaⅠ和RsaⅠ两种四碱基酶进行ARDRA(amplified rDNA restriction analysis)分析。统计比较分析发现,文库a的Shannon-Wienner指数、Simpson指数、丰富度、均一度分别为4.432、0.987、18.885和0.973,均高于文库b中相应的多样性参数(分别为2.271、0.758、5.736和0.501),即平板培养方法所展现的细菌群落结构多样性低于土壤中原始的多样性。结果表明,传统培养方法存在着很大的局限性,必须结合新的分子生物学技术手段才能更全面完善地认识土壤微生物群落结构多样性,以期充分利用其中丰富的微生物资源。     

土壤微生物多样性的分子生态学研究方法

传统的平板培养法分离培养和鉴定土壤微生物只能反映极少数微生物的信息,种类只占土壤微生物种类总数的0.1%～1%,分子生态学方法应用于土壤微生物的鉴定显示出极大的优越性.着重阐述了土壤微生物多样性的研究内容、意义及目前的采用分子生态学的方法研究土壤微生物多样性,尤其以DGGE（denaturing gradient gel electrophoresis）分子生物学技术以及RAPD（Random amplified polymorphic DNA ）随机扩增的多态性分析方法更为精确和快速,为土壤微生物多样性研究提供了一个更加广阔的前景.     

Replant diseases: Bacterial community structure and diversity in peach rhizosphere as determined by metabolic and genetic fingerprinting

Peach tree replant disease, though reported on in the literature for more than two centuries, has yet to have its causes clearly defined. Decline in peach productivity has been attributed to toxic agents, insects, nutritional disturbances, spray residues, fungi and nematodes. Bacteria has also been indicated as a contributing factor.Peach replant disease was reproduced by using two successive cultures on the same soil. Bacterial communities were isolated and characterized from healthy and diseased peach trees. The potential role of cyanide production by rhizobacteria in the replant problem of peaches was studied. Culture-dependent (evaluation of the number of culturable bacteria, metabolic activities, Biolog^® GN2) and independent (ribosomal intergenic spacer analysis, RISA) methods were used, in order to compare bacterial community structure and diversity in healthy and sick soils and to evaluate the possible role of cyanide.Bacterial densities were significantly increased in sick soils. Metabolic activities (Biolog^® GN2) and genetic structure, observed through RISA, were also significantly modified in sick soils. Changes in the composition of individual microbial groups in the rhizosphere of peach trees excavated from healthy or sick soil indicated the involvement of rhizobacteria in the etiology of the replant sickness of peach soil. More than 60% of the strains isolated from healthy soils corresponded to Pseudomonas sp. and 58% of the isolates from sick soils were Bacillus sp. This study determined that Bacillus were able to produce in vitro HCN. It also appeared that in sick soil, there was a shift in the structure of bacterial communities with an increase noted in phytotoxic microorganisms capable of producing HCN compounds.     

Diversity of Paenibacillus durus strains isolated from soil and different plant rhizospheres evaluated by ARDRA and gyrB-RFLP analysis

Strains belonging to Paenibacillus durus isolated from the rhizosphere of various grasses and from bulk soil were previously divided into five phenotypic groups (A1–A5) based on the fermentation pattern of six carbohydrates (A1: sorbitol (+), A2: dulcitol and tagatose (+), A3: starch and glycogen (+), A4: starch, glycogen and d-arabitol (+) and A5: negative for these carbohydrates). This study aimed to assess whether plant types select for specific P. durus phenotypic groups. For that purpose, polymerase chain reaction-restriction fragment length polymorphism analysis of part of genes encoding 16S rRNA (ARDRA) and DNA gyrase subunit B (gyrB-RFLP) were used to produce genetic fingerprints. ARDRA and gyrB-RFLP data were clustered together to generate a dendrogram and two main clusters were observed. Cluster I showed a predominance of strains isolated from wheat, maize and sugarcane rhizospheres. Strains isolated from maize were distributed among the five patterns of carbohydrate metabolism, while strains isolated from sugarcane showed to be predominantly able to metabolize starch and glycogen. Neither sorbitol- nor arabitol-metabolizing strains were found in cluster II, which consisted of strains isolated from soil and from all plant species used. Our results suggest that the plants influenced the diversity of P. durus in their rhizospheres.     

Impact of fumigation with metam sodium upon soil microbial community structure in two Japanese soils

The effects of fumigation with sodium methyl dithiocarbamate (metam sodium) on the microbial community structure and function in 2 soils were investigated using a variety of techniques. In both soils ca. 50% and 90% of the populations of total and culturable bacteria, respectively, were killed by fumigation, with recovery to levels prevailing in control soils 26 d after cessation of fumigation. The size of the ammonium and nitrite oxidiser populations was reduced by up to 4 orders of magnitude by fumigation, with the latter showing a slight recovery 105 d later. There were substantial changes in the C-utilisation (Biolog GN) profiles in the fumigated soils even 105 d later. The number and pattern of amplified 16S ribosomal DNA restriction analysis (ARDRA) fragments was changed by fumigation, and there was a shift in the %G+C profile toward a greater proportion of lower %G+C classes in treated soils. It appeared that DNA released from killed cells remained for some time after fumigation, and masked the apparent community DNA profiles. This study demonstrates that the effects of fumigation on the soil microbial community structure and function were pronounced and for some parameters very persistent. However, the effects on broad-scale properties such as total or culturable bacterial numbers were less enduring.     

思茅松毛虫6龄幼虫肠道细菌的ARDRA分析与鉴定

从自然种群的思茅松毛虫(Dendrolimus kikuchii Matsumura)6龄幼虫肠道环境中分离、纯化、培养获得了6株细菌.以细菌基因组DNA为模板进行PCR扩增,用2种双酶组合Hae Ⅲ和Hin d Ⅲ、HinfⅠ和TaqⅠ对PCR产物进行核糖体DNA扩增片段限制性内切酶分析(ARDRA),得到了3个操作分类单元(OTUs).对每个操作分类单元(OTU)的代表菌株进行16 S rDNA序列测定,序列分析结果表明,分离到的6株肠道细菌中,6N01、6N02、6N03、6N04和6N05属于芽孢杆菌属(Bacillus sp.),6N06属于克雷伯氏杆菌属(Klebsiella sp.).     

3龄思茅松毛虫幼虫肠道好氧细菌的分离及ARDRA多态性分析

从3龄思茅松毛虫(Dendrolimus kikuchii)幼虫肠道样品中分离得到11株好氧细菌.以细菌基因组DNA为模板,扩增16 S rDNA,并用4种限制性内切酶HaeⅢ和HindⅢ、HinfⅠ和TaqⅠ对PCR扩增产物进行ARDRA多态性分析.对聚类图谱的分析结果发现11株好氧细菌在70％的遗传相似度水平上聚成4个不同分类操作单元(OTU),表明3龄松毛虫中肠道内好氧细菌的遗传多样性水平偏低.     

转基因作物对土壤微生物多样性影响研究技术的进展

土壤微生物的多样性是保持农业生态系统稳定的基础,而作物的改变对土壤微生物的多样性结构具有显著的影响.转基因作物被引入到农田后所带来的微生物群落变化及对农业生态系统所带来的不确定因素,已成为研究热点.本文着重介绍了当前土壤微生物多样性研究中常用的3种基于16S rDNA的技术:变性梯度凝胶电泳(DGGE)、扩增性核糖体DNA限制酶切片段分析(ARDRA)和末端限制性酶切片段长度多态性(T-RFLP)技术,分析比较了各种技术的原理、优点及其应用局限性,并简短综述了这些技术近年来的应用.     

Long-term cattle manure application in soil. II. Effect on soil microbial populations and community structure

Studies were conducted to evaluate microbial populations and community structures in soils under different management systems in a long-term continuous winter wheat experiment. These soils had been treated with cattle manure for over a century, and P, NP, NPK, or NPK plus lime for over 70 years. Cattle manure application promoted the growth of bacteria, but not fungi, when compared with the control soil. Application of chemical fertilizers enriched the K-strategist bacterial community, while application of manure enriched both r- and K-strategists. DNA recovered was most abundant in the manure-treated soil. Effects on bacterial species richness and evenness following long-term soil treatments were also demonstrated by analyzing bacterial community DNA using amplified ribosomal DNA restriction analysis and repetitive extragenic palindromic-polymerase chain reaction fingerprinting. The richness and evenness of the bacterial community were enhanced by manure treatment and treatments that included N and P, which were positively correlated with soil productivity.