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1.
土壤微生物是陆地生态系统重要的分解者和地上–地下相互作用的纽带。本文以亚热带杉木(Cunninghamia lanceolateata)人工林为对象,通过模拟林冠层氮沉降和林下灌草去除,设置4种处理,包括:对照(CK)、灌草去除(UR)、氮沉降(N)和氮沉降加灌草去除(N×UR)的野外控制实验,研究土壤微生物群落结构的响应。本实验分别于2016年4月(春季)和10月(秋季)采集0–10cm层土壤样品,运用磷脂脂肪酸法(PLFAs)分析土壤微生物群落结构。结果表明:(1)10月份土壤微生物总PLFAs量及其他类群土壤微生物PLFAs量显著高于4月份(P 0.05),真菌/细菌比值没有显著差异。土壤微生物PLFAs中细菌占优势,其次为真菌,放线菌的占比最小;(2)相比CK处理, UR处理下土壤微生物总PLFAs量、细菌PLFAs量、革兰氏阴性菌PLFAs量和放线菌PLFAs量有增加趋势,但未达到显著差异水平(P 0.05);(3)相对CK, UR、N和N×UR处理降低了4月份土壤微生物多样性(H′)和均匀度指数(J),但提高了10月份土壤微生物多样性指数;(4)冗余分析表明,土壤硝态氮和总磷含量与土壤微生物群落之间呈现显著相关。本研究表明土壤微生物PLFAs在各处理下都表现出明显的季节动态;短期内林下灌草去除对土壤微生物PLFAs影响表现出一定的促进作用,氮沉降对土壤微生物群落影响还不甚明显,需要长期的监测研究来评估两者及其交互作用对土壤微生物群落及其功能的影响。  相似文献   

2.
川西亚高山不同林龄云杉人工林土壤微生物群落结构   总被引:4,自引:0,他引:4  
以川西亚高山云杉人工林林地土壤为对象,采用磷脂脂肪酸(PLFA)法研究了4种不同林龄(50、38、27和20年)的人工林土壤微生物多样性和群落结构特征.结果表明: 随着林龄的增加,土壤有机碳和全氮含量逐步增加;土壤微生物Shannon多样性和Pielou均匀度指数则呈现先增后减的趋势.土壤微生物总PLFAs量、细菌PLFAs量、真菌PLFAs量、放线菌PLFAs量以及丛枝菌根真菌PLFAs量均表现为随林龄的增加而增加.主成分分析(PCA)表明,不同林龄人工林的土壤微生物群落结构之间存在显著差异,其中,第1主成分(PC1)和第2主成分(PC2)共同解释了土壤微生物群落结构总变异的66.8%.冗余分析(RDA)表明,对土壤微生物群落结构产生显著影响的环境因子分别为土壤有机碳、全氮、全钾以及细根生物量.随着人工造林时间的延长,土壤肥力和微生物生物量增加,森林生态系统的恢复进程稳定.  相似文献   

3.
以我国南亚热带格木人工纯林为研究对象,采用气压过程分离(BaPS)技术和磷脂脂肪酸(PLFAs)法研究了不同枯落物处理(对照、枯落物去除、枯落物加倍)下土壤碳氮转化速率和微生物群落结构的季节变化.结果表明:不同枯落物处理土壤呼吸和总硝化速率均呈现明显的季节动态,雨季显著高于旱季.枯落物处理初期,土壤呼吸和总硝化速率均随枯落物输入量的增加呈下降趋势,但随着枯落物处理时间的延长,二者随枯落物输入量的增加而增加.旱季不同枯落物处理土壤微生物PLFAs总量和各菌群PLFAs量均显著高于雨季,而雨季真菌PLFAs/细菌PLFAs明显高于旱季.在旱季,枯落物去除处理土壤微生物PLFAs总量、细菌PLFAs量、真菌PLFAs量和丛枝菌根真菌PLFAs量分别显著提高30.9%、28.8%、44.4%和31.6%.在雨季,枯落物去除处理细菌PLFAs量和丛枝菌根真菌PLFAs量分别显著降低10.6%和33.3%.土壤微生物群落结构受枯落物输入量处理和季节的双重影响,土壤微生物群落结构主要受土壤温度和铵态氮的影响.枯落物输入量处理在短期内显著影响了格木林土壤碳氮转化速率和微生物群落结构,这种影响因季节的不同而存在差异.  相似文献   

4.
杉木人工林土壤微生物群落结构特征   总被引:10,自引:0,他引:10  
采用氯仿熏蒸法、稀释平板法和磷脂脂肪酸(phospholipid fatty acid,PLFA)方法,分析了常绿阔叶林转变成杉木人工林后土壤微生物种群数量和群落结构的变化特征.结果表明:常绿阔叶林转变为杉木人工林后,林地土壤的微生物生物量碳、可培养细菌和放线菌数降低.杉木人工林地总PLFAs、细菌PLFAs、真菌PLFAs比常绿阔叶林分别降低了49.4%、52.4%和46.6%,革兰氏阳性和阴性细菌PLFAs远低于常绿阔叶林.杉木人工林根际土壤微生物生物量碳、可培养细菌和放线菌数显著高于杉木人工林林地土壤,根际土壤中总PLFAs、细菌PLFAs、革兰氏阳性和阴性细菌PLFAs的含量也高于林地土壤,但真菌PLFAs和细菌PLFAs之比却低于林地土壤.对土壤微生物群落结构进行主成分分析发现,第1主成分和第2主成分共解释了土壤微生物群落结构变异的78.2%.表明常绿阔叶林与杉木人工林土壤的微生物群落结构间存在差异.  相似文献   

5.
凋落物管理对樟子松人工林土壤微生物群落结构的影响   总被引:1,自引:0,他引:1  
采用磷脂脂肪酸法(PLFA)分析短期(18个月)凋落物管理对樟子松人工林土壤微生物群落结构的影响。结果表明,凋落物移除对土壤各类微生物的PLFAs均无显著影响,但凋落物加倍显著改变了土壤微生物群落结构。凋落物加倍显著提高了土壤PLFAs总量、革兰氏阳性细菌(G+)与革兰氏阴性细菌(G-)和原生动物PLFAs,但对真菌和放线菌PLFAs以及细菌/真菌值、G+/G-值影响不显著。凋落物加倍使土壤总PLFAs上升了82.4%,细菌PLFAs上升了93.9%。凋落物管理对樟子松人工林土壤微生物的Shannon多样性指数、Pielou均匀度指数和Simpson优势度指数均无显著影响。主成分分析表明,主成分1(89.83%)上得分系数较高的PLFAs多为细菌的特征PLFAs,主要有16:1ω5c、16:1ω7c、cy17:0ω7c、cy19:0ω7c、i14:0、i15:0。  相似文献   

6.
嫁接辣椒根系特征及根际土壤酶活性与青枯病抗性的关系   总被引:1,自引:0,他引:1  
以‘卫士’辣椒为砧木,‘新丰2号’为接穂嫁接,通过人工接种青枯病菌研究嫁接和自根辣椒根系特征、根际土壤微生物及酶活性的变化,探讨嫁接辣椒的抗病机理.结果显示:接种青枯病菌前,嫁接辣椒的根系重量、总长度、总体积、表面积、根尖数和分叉数均显著高于自根苗,根系活力、根际土壤放线菌数量和比例,以及根际土壤酶(多酚氧化酶、过氧化物酶和脱氢酶)活性也明显高于自根苗.接种青枯病菌后,嫁接辣椒的根系受伤程度较自根苗轻,根系重量、总长度、总体积、表面积、根尖数和分叉数的降低幅度均显著小于自根苗,根系活力、根际土壤微生物数量、放线菌比例及土壤酶活性明显大于自根苗.研究表明,嫁接辣椒根系发达,根系活力增强,根际土壤放线菌比例增加及酶活性提高是其青枯病抗性增强的重要原因.  相似文献   

7.
研究了干旱生境下接种假单胞菌YT3、枯草芽孢杆菌DZ1、蜡样芽孢杆菌L90和纺锤芽孢杆菌L13等4株植物根际促生细菌(PGPR)对核桃根际土壤生物学特征的影响.结果表明:干旱对核桃根际土壤养分有效性影响不显著,但高活性有机碳含量降低18.4%,pH由7.34显著提高到7.79.干旱生境下接种L90后,土壤高活性有机碳含量提高14.5%,pH降低至7.41.干旱导致根际土壤微生物总量、微生物生物量碳、氮和根系分泌物含量分别下降36.0%、20.7%、33.5%和30.7%,接种L90后仅分别降低14.1%、10.3%、12.1%和12.7%.核桃根际土壤微生物的末端限制性片段长度多态性分析图谱显示,干旱胁迫导致一些优势细菌群落消失,而接种PGPR对核桃根际土壤细菌群落结构有较大影响.干旱胁迫下核桃根际土壤微生物群落的Margalef指数和Shannon指数显著降低,Simpson指数显著增加;接种L90后,Margalef指数和Shannon指数分别由0.42和0.52增至0.99和0.98,Simpson指数由0.60降至0.39.与接种L90处理相比,干旱生境下接种YT3、DZ1和L13处理核桃根际土壤生物学特征差异不显著,表明L90可有效抑制干旱引起的核桃根际土壤生物学特征的改变.  相似文献   

8.
耕作方式对潮土土壤团聚体微生物群落结构的影响   总被引:1,自引:0,他引:1  
为探究不同耕作方式对潮土土壤团聚体微生物群落结构和多样性的影响,采用磷脂脂肪酸(PLFA)法测定了土壤团聚体中微生物群落。试验设置4个耕作处理,分别为旋耕+秸秆还田(RT)、深耕+秸秆还田(DP)、深松+秸秆还田(SS)和免耕+秸秆还田(NT)。结果表明:与RT相比,DP处理显著提高了原状土壤和>5 mm粒级土壤团聚体中真菌PLFAs量和真菌/细菌,为真菌的繁殖提供了有利条件,有助于土壤有机质的贮存,提高了土壤生态系统的缓冲能力;提高了5~2 mm粒级土壤团聚体中细菌PLFAs量,降低了土壤革兰氏阳性菌/革兰氏阴性菌,改善了土壤营养状况;提高了<0.25 mm粒级土壤团聚体中微生物丰富度指数。总的来说,深耕+秸秆还田(DP)对土壤团聚体细菌和真菌生物量有一定的提高作用,并且在一定程度上改善了土壤团聚体微生物群落结构,有利于增加土壤固碳能力和保持土壤微生物多样性。冗余分析结果表明,土壤团聚体总PLFAs量、细菌、革兰氏阴性菌和放线菌PLFAs量与土壤有机碳相关性较强,革兰氏阳性菌PLFAs量与总氮相关性较强。各处理较大粒级土壤团聚体微生物群落主要受碳氮比、含水量、pH值和团聚体质量分数的影响,较小粒级土壤团聚体微生物群落则主要受土壤有机碳和总氮的影响。  相似文献   

9.
为了明确土壤微生物群落组成和结构对草原灌丛平茬处理的响应,并分析土壤微生物群落组成、结构与土壤理化性质及地上部植物群落的关系,本研究以小叶锦鸡儿灌丛化的退化草原为对象,对小叶锦鸡儿灌丛实施平茬处理并设置未平茬对照,处理3个月后,对两种处理条件下灌丛间植物群落的组成和结构及土壤理化性质进行测定,并运用磷脂脂肪酸(phospholipid fatty acid,PLFA)生物标记法分析两种处理下0~5和15~20 cm土层土壤微生物群落组成和结构。结果显示:(1)与对照相比,平茬样方植物群落地上总生物量有下降趋势,主要表现在褐沙蒿生物量的下降,物种数及Shannon指数显著增加,0~5 cm土壤p H显著降低,而15~20 cm土壤全碳、全氮及碳氮比显著提高; 0~5 cm土壤总PLFAs、格兰氏阳性菌(G~+)、格兰氏阴性菌(G~-)、细菌(B)、真菌(F)以及放线菌(Act) PLFAs含量显著增加,G~+/G~-显著降低。(2)冗余分析结果表明,土壤p H与G~+PLFAs含量呈正相关,与G~-、F及Act PLFAs含量呈负相关;土壤全氮与G~+、G~-、F及Act PLFAs含量均呈正相关;Shannon指数与G~+PLFAs含量呈负相关,与G~-、F及Act PLFAs含量呈正相关;地上总生物量与G~-、F及Act PLFAs含量呈负相关。这些结果表明了土壤微生物群落组成和结构能够对草原灌丛平茬处理引起的地上部植物群落及土壤环境条件的变化快速响应,对土壤健康状况具有指示作用,可为内蒙古灌丛化草原的恢复提供科学指导。  相似文献   

10.
以山西省长治市潞安矿区煤矸山复垦多年的林地和草地为对象,采用磷脂脂肪酸法(phospholipid fatty acid,PLFA)研究2种复垦样地0~10和10~20 cm土层土壤微生物多样性和群落组成状况以及土壤环境因子对微生物群落组成的影响。结果表明:(1)草地0~10和10~20 cm土层土壤微生物丰富度指数(S)、Shannon指数(H)均大于林地(P0.05),但2种样地Pielou均匀度指数(E)无显著差异。(2)林地在0~10和10~20 cm土层土壤微生物总PLFAs含量、真菌PLFAs含量、放线菌PLFAs含量、革兰氏阳性菌PLFAs含量以及革兰氏阳性菌/革兰氏阴性菌、真菌/细菌均高于草地(P0.05);但细菌PLFAs含量和革兰氏阴性菌PLFAs含量在2土层中表现不同,林地0~10 cm土层高于草地(P0.05),10~20 cm土层则低于草地。(3)主成分分析表明,土壤微生物群落结构组成受复垦类型的显著影响。冗余分析表明,土壤理化性质对微生物PLFAs含量产生影响,其中土壤有效磷(AP)、pH值和阳离子交换量(CEC)是影响微生物群落组成的主要因子,并且AP和CEC与土壤微生物PLFAs含量呈正相关,pH值与之呈负相关。  相似文献   

11.
AM真菌对青枯菌和根际细菌群落结构的影响   总被引:12,自引:0,他引:12  
利用传统的平板培养与DGGE相结合的技术手段,研究了接种AM真菌对番茄根际土壤中的青枯菌和细菌群落结构的影响。结果表明,菌根根际土壤中的细菌总量和总DNA量都高于非菌根根际土壤,其中前者的青枯菌种群数量比后者低60倍;DGGE图谱也证实了AM真菌对青枯菌的抑制效应,还揭示出接种AM真菌对根际土壤中细菌群落结构所产生的复杂的影响。文章对AM真菌抑制青枯菌的机制进行了探讨。  相似文献   

12.
Bacterial wilt, caused by Ralstonia solanacearum, is a serious disease of tobacco in North and South Carolina. In contrast, the disease rarely occurs on tobacco in Georgia and Florida, although bacterial wilt is a common problem on tomato. We investigated whether this difference in disease incidence could be explained by qualitative characteristics of avirulence gene avrA in the R. solanacearum population in the southeastern United States. Sequence analysis established that wild-type avrA has a 792-bp open reading frame. Polymerase chain reaction (PCR) amplification of avrA from 139 R. solanacearum strains generated either 792-bp or approximately 960-bp DNA fragments. Strains that elicited a hypersensitive reaction (HR) on tobacco contained the 792-bp allele, and were pathogenic on tomato and avirulent on tobacco. All HR-negative strains generated a approximately 960-bp DNA fragment, and wilted both tomato and tobacco. The DNA sequence of avrA in six HR-negative strains revealed the presence of one of two putative miniature inverted-repeat transposable elements (MITEs): a 152-bp MITE between nucleotides 542 and 543, or a 170-bp MITE between nucleotides 461 and 462 or 574 and 575. Southern analysis suggested that the 170-bp MITE is unique to strains from the southeastern United States and the Caribbean. Mutated avrA alleles were present in strains from 96 and 75% of North and South Carolina sites, respectively, and only in 13 and 0% of the sites in Georgia and Florida, respectively. Introduction of the wildtype allele on a plasmid into four HR-negative strains reduced their virulence on both tobacco and tomato. Inactivation of avrA in an HR-positive, avirulent strain, resulted in a mutant that was weakly virulent on tobacco. Thus, the incidence of bacterial wilt of tobacco in the southeastern United States is partially explained by which avrA allele dominates the local R. solanacearum population.  相似文献   

13.
Ralstonia solanacearum biovar 2, the causative agent of brown rot in potato, has been responsible for large crop losses in Northwest Europe during the last decade. Knowledge on the ecological behaviour of R. solanacearum and its antagonists is required to develop sound procedures for its control and eradication in infested fields.A polyphasic approach was used to study the invasion of plants by a selected R. solanacearum biovar 2 strain, denoted 1609, either or not in combination with the antagonistic strains Pseudomonas corrugata IDV1 and P. fluorescens UA5-40. Thus, this study combined plating (spread and drop plate methods), reporter gene technology (gfp mutants) and serological (imunofluorescence colony staining [IFC]) and molecular techniques (fluorescent in situ hybridization [FISH], PCR with R. solanacearum specific primers and PCR-DGGE on plant DNA extracts). The behaviour of R. solanacearum 1609 and the two control strains was studied in bulk and (tomato) rhizosphere soil and the rhizoplane and stems of tomato plants.The results showed that an interaction between the pathogen and the control strains at the root surface was likely. In particular, R. solanacearum 1609 CFU numbers were significantly reduced on tomato roots treated with P. corrugata IDV1(chr:gfp1) cells as compared to those on untreated roots. Concomitant with the presence of P. corrugata IDV1(chr:gfp1), plant invasion by the pathogen was hampered, but not abolished.PCR-DGGE analyses of the tomato rhizoplane supported the evidence for antagonistic activity against the pathogen; as only weak R. solanacearum 1609 specific bands were detected in profiles derived from mixed systems versus strong bands in profiles from systems containing only the pathogen. Using FISH, a difference in root colonization was demonstrated between the pathogen and one of the two antagonists, i.e. P. corrugata IDV1(chr:gfp1); R. solanacearum strain 1609 was clearly detected in the vascular cylinder of tomato plants, whereas strain IDV1 was absent.R. solanacearum 1609 cells were also detected in stems of plants that had developed in soils treated with this strain, even in cases in which disease symptoms were absent, indicating the occurrence of symptomless infection. In contrast, strain 1609 cells were not found in stems of several plants treated with either one of the two antagonists.The polyphasic analysis is valuable for testing antagonistic strains for approval as biocontrol agents in agricultural practice.  相似文献   

14.
摘要:【目的】采用根系分泌物培养基筛选到一株番茄根际优势细菌YPP-9。本文分析测定该菌株对植物青枯病菌茄科雷尔氏菌的拮抗作用和控病能力,及其在番茄根际的定殖能力,并系统分析该菌株的分类学地位。【方法】以平板双重培养法和温室盆栽试验分别测定菌株对病原菌的拮抗能力和对番茄青枯病的控病能力;利用变性梯度凝胶电泳技术分析菌株在番茄根际的定殖能力;以形态学和生理生化特性以及16S rRNA基因序列分析确定菌株的分类地位。【结果】菌株YPP-9对茄科雷尔氏菌SSF-4的平板抑菌带宽为5 mm,其盆栽控制番茄青枯病的效果达63.7%。菌株YPP-9在番茄根际具有较好的定殖能力。该菌株培养24 h后菌落呈奶酪色,革兰氏染色阳性,菌体杆状、大小1.8-4.1 μm×0.9-1.1 μm,形成芽孢,芽孢中生或偏端生且为近似柱形,孢囊不膨大,无伴孢晶体,侧生鞭毛。菌株生长pH范围为pH 5.5-8.5且最适生长pH为6.0,生长温度范围为20℃-45℃且最适生长温度为30℃。The BIOLOG GP2结果显示该菌为芽孢杆菌属。16S rRNA基因序列分析显示该菌株与Bacillus fumarioli的亲缘关系最近且序列相似性为97%,且其序列号为FJ231500。该菌株的G+C含量为41.9%,甲基萘醌主要类型为MK-7,细胞壁脂肪酸的主要种类为C14:0 iso、C15:0 iso 和C16:0 iso以及C16 : 1ω7c alcohol且含量分别为28.27%、19.59%、12.93%和10.88%。【结论】菌株YPP-9对茄科雷尔氏菌具有良好的拮抗作用和盆栽控病能力,且能良好的定殖于番茄根际。分类学上,该菌株归入芽胞杆菌属(Bacillus),并可能是一个新的种。  相似文献   

15.
Li Z  Wu S  Bai X  Liu Y  Lu J  Liu Y  Xiao B  Lu X  Fan L 《Journal of bacteriology》2011,193(21):6088-6089
Ralstonia solanacearum is a causal agent of plant bacterial wilt with thousands of distinct strains in a heterogeneous species complex. Here we report the genome sequence of a phylotype IB strain, Y45, isolated from tobacco (Nicotiana tabacum) in China. Compared with the published genomes of eight strains which were isolated from other hosts and habitats, 794 specific genes and many rearrangements/inversion events were identified in the tobacco strain, demonstrating that this strain represents an important node within the R. solanacearum complex.  相似文献   

16.
[目的]研究青枯病病原菌与拮抗菌的营养特性及其对烟草根系分泌物的响应差异,对提高拮抗菌定殖能力、有效生物防控烟草青枯病具有非常重要的意义。[方法]本研究通过筛选与鉴定贵州烟区青枯病病原菌株及拮抗菌株,通过Biolog表型芯片技术分别检测病原菌与拮抗菌的特征性碳、氮源,利用气质联用(GC-MS)检测烟草主栽品种K326根系分泌物的主要物质,在此基础上进行病原菌与拮抗菌对其利用能力、利用强度以及共培养的研究。[结果]经鉴定,分离、筛选到的病原菌株和拮抗菌株分别为青枯劳尔氏菌(Ralstonia solawacearum)和枯草芽孢杆菌(Bacillus subtilis);在含量为0.01μg/mL以上的根系分泌物中,12种物质的含量从高到低排序为:果胶>葡萄糖>木糖>阿拉伯糖>半乳糖>核糖>蔗糖>苯甲酸>果糖=D-甘露醇>棕榈酸>富马酸,果胶含量最高且明显高于其他物质;拮抗菌(LX4)对碳源利用能力高于病原菌(Rs)的碳源有阿拉伯糖、木糖和核糖,分别是病原菌利用能力的1.22、1.95和2.17倍;前12 h拮抗菌利用果糖强度高于病原菌,不同碳源共培养24 h后LX4对gfp-Rs(绿色荧光蛋白标记后的青枯病病原菌)抑制率为18.34%(阿拉伯糖)、53.23%(木糖)、63.53%(核糖)和52.09%(果糖)。[结论]拮抗菌对烟草根系分泌物的利用不及病原菌,但在特定碳源条件下拮抗菌能够利用根系分泌物中的某些碳源产生某种拮抗物质抑制病原菌,拮抗菌与病原菌之间同时存在利用性竞争和干扰性竞争关系,研究结果为进一步研究烟草青枯病的生物防控提供了新的理论依据。  相似文献   

17.
Bacterial wilt caused by Ralstonia (formerly Pseudomonas) solanacearum is worldwide in distribution. It is one of the most destructive bacterial diseases of economically important crops. The serological assays so far developed for the detection of R. solanacearum were able to provide information as to the presence or absence of the pathogen in soil and plant materials. However, they could not discriminate between virulent and avirulent strains of the pathogen and were not specific to strains and races. In the present investigation, virulent bacterial cells (encapsulated with mucin) from tomato seeds were used as antigen and polyclonal antisera were developed in rabbit using a classical immunization protocol. Antisera thus developed were examined for the antibody titre, sensitivity, specificity, rapidity and the efficacy of the antibody in identifying the virulent and avirulent strains of the pathogen and the potential for application of this assay to the screening of infected plant materials and seeds. Our results indicate that the anti-tomato R. solanacearum: (i) has a good antibody titre of 1:10,000; (ii) can detect as few as 100 bacterial cells/ml; (iii) is tomato-specific (it reacted with tomato R. solanacearum, and not with isolates from chilli or eggplant); (iv) is reactive to all isolates of R. solanacearum from tomato; (v) is not cross-reactive with non-pseudomonads; (vi) is virulent strain-specific as it recognizes the virulent exopolysaccharide component as an antigenic determinant; (vii) reactivity could be correlated well with the degree of infection in tomato seeds and plant materials. The enzyme linked immunosorbent assay developed is sensitive, specific and rapid, therefore suitable for the detection of R. solanacearum isolates from tomato seeds during routine assays.  相似文献   

18.
【目的】为了控制烟草疫霉(Phytophthora nicotianae)引起的烟草黑胫病对烟草生产造成的危害。【方法】采用稀释平板法从贵州省毕节地区烟草根际土壤中分离筛选拮抗烟草疫霉的细菌菌株,然后经形态观察、Biolog鉴定及16S rRNA基因序列分析,对分离菌株进行鉴定,同时测定抗菌谱,单因子变量分析、优化生长条件。【结果】共分离得到44株拮抗烟草疫霉的细菌菌株,其中菌株21b对烟草黑胫病菌菌丝生长的抑制率达78.33%,鉴定为枯草芽孢杆菌(Bacillus subtilis)。该菌株对烟草青枯病菌(Ralstonia solanacearum)、烟草灰霉病菌(Botrytis cinerea)、烟草赤星病菌(Alternaria alternate)和烟草炭疽病菌(Colletotrichum destructivum)均具有拮抗作用,抑菌圈大小分别为19.5、18.2、14.6和13.4 mm,最佳的发酵条件为:温度30°C、p H 7.0–8.0、装液量12%、盐浓度0.5%。【结论】分离筛选到一株对烟草寄生疫霉有较强拮抗活性的细菌菌株,为进一步开发烟草黑胫病的生防菌剂提供了菌种资源。  相似文献   

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