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1.
马铃薯干腐病菌和黑痣病菌拮抗芽胞杆菌的筛选及鉴定   总被引:2,自引:0,他引:2  
从甘肃国营条山农场马铃薯连作试验田的96个小区以五点取样法采集根际土样,稀释平板法在LB培养基上分离得到625株芽胞杆菌菌株。统计分析表明,土壤中总芽胞杆菌的数量正茬〉连作2年〉连作4年,但连作6年的土壤中总芽胞杆菌的数量又有上升的趋势。以马铃薯干腐病菌接骨木镰刀菌FusariumsambucinumFSM、茄病镰刀菌FsolaniFSI、黑痣病菌立枯丝核菌RhizoctoniasolaniRSl和RS2为靶标病原菌,平板对峙培养法筛选有抑菌效果的拮抗芽胞杆菌,发现抑菌带宽度大于2mm的拮抗芽胞杆菌的数量随连作年限的增加而减少。以形态学特征、生理生化特性为基础,结合gyrB基因序列分析,将筛选出的2株拮抗效果较好且不引起马铃薯块茎腐烂的芽胞杆菌Bacillusspp.D1—0—1和D1—0—2鉴定为萎缩芽胞杆菌B.atrophaeus。  相似文献   

2.
王春明  郭成  周天旺  洪流 《植物保护》2023,49(4):256-262
为了明确一种引起玉米叶片腐烂的细菌性病害的病原菌种类, 于2021年7月在甘肃省景泰县条山农场玉米种植区采集病样, 经稀释分离法进行病原菌分离纯化, 并通过致病性测定?形态学观察?生理生化特征观察及16S rDNA和gyrB序列分析相结合的方法对病原菌进行鉴定?结果表明, 选取的代表性菌株B1-0和B2-1均能使玉米叶片发病, 为革兰氏阳性致病菌, 产芽胞; 该病原菌需氧性?运动性?明胶液化?接触酶试验?柠檬酸盐利用?马铃薯腐烂试验均为阳性; 甲基红试验阴性; 能利用D-甘露醇?麦芽糖和葡萄糖, 不能利用甘油和肌醇, 不能水解淀粉, 在4℃?40℃和5%NaCl条件下均能生长?构建基于16S rDNA和gyrB的系统发育树, B1-0和B2-1与短小芽胞杆菌Bacillus pumilus(ATCC7061?BKS1-108?AUEC29?BP-hd-1?NMTD17和17)亲缘关系最近, 聚在一个分支?因此, 将该病原菌鉴定为短小芽胞杆菌B. pumilus?研究结果将为玉米细菌性叶部病害的研究和综合防治提供基础数据?  相似文献   

3.
为明确引起四川理县大白菜软腐病的病原菌种类, 从理县梭罗沟村田间采集具有典型软腐症状的大白菜病样, 采用组织分离、致病力测定、生理生化分析、形态学和分子生物学方法进行鉴定。结果表明, 分离获得的5株细菌在NA培养基上形成的菌落呈圆形、半透明、乳白色、中心突起、边缘平滑, 在半选择性培养基CVP上培养48 h后产生凹陷。5株菌均能使大白菜、胡萝卜、马铃薯和芹菜的离体组织腐烂, 接种于白菜苗后叶片呈湿腐萎蔫症状。通过大白菜叶柄接种部位形成的病斑长径来比较菌株致病力强弱, 各菌株的致病力有显著差异。基于看家基因pgi、rpoS、mdh、proA、mtlD 和icdA(NCBI登录号为OL963562~OL963571)的多基因联合系统发育树, 分离菌株与Pectobacterium versatile聚为一簇, dnaX-leuS-recA(NCBI登录号为OL963572~OL963576)的多位点序列分析(MLSA)进一步支持以上结果, 且准确性更高。分离菌株的生理生化特征与P.versatile模式菌株一致, 综上将其鉴定为P.versatile。这是我国首次报道P.versatile引起大白菜软腐病。  相似文献   

4.
马铃薯块茎病原真菌拮抗菌株筛选及优良拮抗菌株鉴定   总被引:1,自引:0,他引:1  
从马铃薯块茎上分离内生细菌,以块茎病原真菌为指示菌,采用平板对峙法筛选拮抗菌株,并利用形态学特征和16S rDNA基因序列分析对优良拮抗菌株进行鉴定。结果表明,从定西马铃薯块茎中共分离得到72株内生细菌,其中19株对5种块茎病原真菌的抑菌率均高于51.87%,特别是内生细菌6-5和5-6分别对马铃薯炭疽病菌Colletotrichum coccodes和马铃薯黑痣病菌Rhizoctonia solani的抑菌率达85.82%和72.18%,且具有固氮和产吲哚乙酸(IAA)功能,其产IAA量分别为3.37 mg/L和19.25 mg/L;根据形态特征及16S rDNA基因序列将菌株5-6鉴定为萎缩芽胞杆菌Bacillus atrophaeus,菌株6-5鉴定为贝莱斯芽胞杆菌Bacillus velezensis。  相似文献   

5.
人参灰霉病拮抗细菌的筛选及鉴定   总被引:1,自引:0,他引:1  
为获取对灰葡萄孢Botrytis cinerea Pers.ex Fr.防效优良的菌株,采用滤纸片法和牛津杯法从105株菌株中筛选出7株拮抗性良好的菌株,采用平板对峙法对抑菌效果较好的菌株SZ-35进行抑菌谱测定,采用盆栽法研究其对人参灰霉病的防效及在人参体内的定殖能力,并通过形态学、生理生化特征、16S rDNA及gyrB基因测序确立其分类地位。结果显示,菌株SZ-35对灰葡萄孢的抑制作用最强,抑菌率和抑菌带宽分别为86.53%和12.20 mm,且具有广谱抑菌能力;菌株SZ-35可有效定殖于人参体内,对人参灰霉病的防效达76.42%,显著高于70%代森锰锌可湿性粉剂;通过形态特征、生理生化特征观察,以及16S rDNA及gyrB同源性序列对比分析,鉴定菌株SZ-35为解淀粉芽胞杆菌Bacillus amyloliquefaciens(GenBank登录号为KC511113)。研究表明,解淀粉芽胞杆菌SZ-35对灰葡萄孢具有良好的抑菌能力,且在人参中的定殖能力较好。  相似文献   

6.
吴慧芳  蒙耀  石晖琴  魏琳  沈硕 《植物保护》2024,50(3):111-120
镰孢菌引起的马铃薯干腐病是影响马铃薯贮存期间产量与品质的重要病害之一。寻找高效低毒的防治马铃薯干腐病的生防药剂对提高马铃薯的产量与质量具有重要意义。本研究以腐皮镰孢Fusarium solani为病原菌, 测定分离自马铃薯块茎的菌株2-1-9-CJK-2的抑菌活性。该菌株发酵液、无菌发酵液、菌悬液、胞内组分以及挥发性有机物对腐皮镰孢均具有抑菌活性, 抑制率分别为93.37%、61.92%、80.82%、44.01%和49.16%。结合形态学、生理生化特征和多基因系统发育树构建鉴定其为贝莱斯芽胞杆菌Bacillus velezensis。马铃薯切片试验和马铃薯块茎试验表明, 当菌株发酵液浓度为1×109 cfu/mL时, 对病原菌的抑制效果最好。除此之外, 菌株可以分泌蛋白酶、淀粉酶、纤维素酶, 具有溶磷能力和生物膜形成能力, 但不具有溶血性, 并且对供试的其他6种病原真菌有较强的抑菌活性。研究表明贝莱斯芽胞杆菌2-1-9-CJK-2抑菌谱广, 具有生物安全性, 对腐皮镰孢有较强的抑菌活性, 在植物病害防治中具有一定的应用潜力, 可为马铃薯干腐病生防制剂的开发奠定基础。  相似文献   

7.
为明确贵州魔芋软腐病菌种类?致病力及分布特点, 采用组织分离法对贵州主要魔芋种植区软腐病样进行病原菌分离, 对icdA, mdh, mtlD, proA, rpoS 等5个管家基因进行了扩增?序列测定, 分别用单基因和多基因联合系统发育树对病菌进行鉴定, 同时采用组织块接种方法测定了不同菌株的致病力?通过组织分离法共分离魔芋软腐病菌株47株; 采用5个管家基因进行分子鉴定, 将病菌分别鉴定为海芋果胶杆菌Pectobacterium aroidearum?胡萝卜果胶杆菌Pectobacterium carotovorum和方中达迪基氏菌Dickeya fangzhongdai 3个种, 其中海芋果胶杆菌P.aroidearum为贵州魔芋软腐病主要致病菌, 占分离菌株的70%, 广泛分布在多个地区; 其次为方中达迪基氏菌D. fangzhongdai, 占分离菌株的28%, 也普遍存在于贵州各魔芋种植区; 胡萝卜果胶杆菌P. carotovorum最少, 占分离菌株的2%?致病力测定结果表明, 菌株间致病力存在一定的差异, 其中海芋果胶杆菌不同菌株之间致病力差异较大, 低?中?高致病力菌株都有, 方中达迪基氏菌差异较小, 仅有中?高致病力菌株?本研究确定了贵州魔芋软腐病菌种类?致病力及在贵州的分布特点, 首次报道了海芋果胶杆菌?方中达迪基氏菌是贵州魔芋软腐病的主要病原菌, 进一步加深了对魔芋软腐病及其发生流行的认识, 为软腐病的科学防控提供了科学依据?  相似文献   

8.
采用对峙培养法对马铃薯炭疽病的拮抗菌株进行了筛选和鉴定。结果表明,拮抗菌株ZHA10对炭疽病病原菌具有良好的抑制作用,抑制率达76.43%,其可以使病原菌菌丝变形和裂解;ZHA10菌体短杆状、革兰氏阳性、大小为(0.5~0.75)μm × (1.5 ~3.1)μm、芽胞中至尖端生。通过生理生化测定、16S rDNA以及gyrB序列分析,鉴定ZHA10为枯草芽胞杆菌(Bacillus subtilis)。此外,ZHA10还对番茄早疫病菌(Alternaria solani)、马铃薯干腐病菌(Fusarium oxysporum)、孜然根腐病菌(Fusarium solani)、小麦根腐病菌(Bipolaris sorokiniana)、黄瓜枯萎病菌(Fusarium oxysporum)和马铃薯褐腐病菌(Stysanus stemonitis)均具有较强的拮抗作用。ZHA10抑菌能力良好,抑菌谱宽,具有进一步开发应用的潜力。  相似文献   

9.
为有效防控十字花科蔬菜生产中的毁灭性病害——根肿病,以尖孢镰孢菌Fusarium oxysporum和辣椒疫霉Phytophthora capsici为指示菌,利用平板对峙法对分离自土壤的1 198株细菌进行筛选,进通过盆栽试验筛选对十字花科根肿病具有良好防效的生防菌株,并基于形态学特征、生理生化特性及16S rDNA、gyrB和atpD多基因系统发育分析对生防菌株进行鉴定,同时测定其抑菌谱和田间防效。结果表明,通过对峙培养筛选获得115株有抑菌效果的生防菌株,采用盆栽试验获得1株对根肿病菌具有拮抗效果的菌株,命名为ZF480。结合形态学特征和系统发育分析结果将该菌株鉴定为副地衣芽胞杆菌Bacillus paralicheniformis。菌株ZF480对野油菜黄单胞野油菜变种Xanthomonas campestris pv. campestris等10种病原菌具有拮抗效果,抑菌谱较宽,对白菜根肿病的盆栽防效和田间防效分别达到72.82%和64.08%。表明副地衣芽胞杆菌菌株ZF480对十字花科根肿病具有显著的防效,可作为生防菌进一步开发利用。  相似文献   

10.
自青海北山林场桦树根围分离筛选到芽胞杆菌菌株166株,根据菌落特征分为6个类群,选择其中31株菌株纯化保存并进行BOX—PCR及ERIC—PCR指纹图谱分析、16SrDNA及gyrB基因序列分析,鉴定出球形赖氨酸芽胞杆菌Lysinibacillussphaericus12株、解淀粉芽胞杆菌Bacillusamyloliq-uefaciens 5株、韦氏芽胞杆菌Bacillusweihenstephanensis7株、芽胞杆菌Bacillussp.5株、苏云金芽胞杆菌Bacillusthuringiensis2株。通过平板对峙试验筛选得到11株对油菜菌核病原真菌Sclerotiniasclerotiorum具有显著拮抗活性的菌株。以MALDI.TOF.MS质谱分析拮抗菌株QBll的活性成分,可产生脂肽化合物表面活性素和泛革素,表明其拮抗活性与脂肽化合物的合成和分泌有关。  相似文献   

11.
为确定引起呼和浩特市苜蓿根腐病的病原菌种类,采用常规组织分离法对采集的疑似苜蓿根腐病病样进行病原菌分离与培养,利用形态学观察结合分子生物学方法对分离物代表菌株进行鉴定,并采用土壤接种法对代表菌株的致病性进行测定。结果表明,共分离获得6类形态学特征不同的分离物,各随机选择1株代表菌株进行鉴定,结合分子生物学鉴定结果确定呼和浩特市苜蓿根腐病病原菌有6种,分别是麦根腐平脐蠕孢菌Bipolaris sorokiniana、立枯丝核菌Rhizoctonia solani、木贼镰刀菌Fusarium equiseti、变红镰刀菌F. incarnatum、锐顶镰刀菌F. acuminatum和织球壳枯萎菌Plectosphaerella cucumerina,分别分离到1、7、14、26、7和14株菌株,占总分离菌株数的1.45%、10.14%、20.29%、37.68%、10.14%和20.29%。其中,立枯丝核菌的致病力最强,接种苜蓿幼苗发病的病情指数达82.67,其次为木贼镰刀菌、变红镰刀菌、锐顶镰刀菌、麦根腐平脐蠕孢菌和织球壳枯萎菌,病情指数分别为72.67、62.67、58.67、52....  相似文献   

12.
Gnomonia fragariae has been occasionally listed among the fungi associated with diseased strawberry plants. However its pathogenicity has not been established. During the investigation on strawberry decline in Latvia and Sweden, a fungus was repeatedly recovered from discoloured root and crown tissues of severely stunted plants. Attempts to induce sporulation of the isolates grown on several agar media resulted in the formation of mature ascomata only on potato carrot agar and oatmeal agar. On morphological grounds and comparisons with reference herbarium specimens these isolates were identified as Gnomonia fragariae. The pathogenicity of the fungus was evaluated initially in the detached leaf assay and subsequently in three bioassays on strawberry plants. All the bioassays showed that G. fragariae was pathogenic on strawberry and capable of causing severe root rot and petiole blight. The symptoms that developed in the greenhouse experiments closely resembled those observed in the fields. The fungus did not cause rapid plant death but growth and development of inoculated strawberry plants was severely affected. To our knowledge this is the first time when pathogenicity of G. fragariae as a root rot pathogen has been clearly established. Our study shows that G. fragariae is one of the serious pathogens involved in the root rot complex of strawberry in Latvia and Sweden.  相似文献   

13.
Foot rot of mature tomato plants was found in four cities of Hokkaido, Japan, from 2004 to 2007. Six of eight isolates obtained from damaged tissues were identified as Rhizoctonia solani anastomosis group (AG)-3, and the remaining two isolates belonged to AG-2-1. We compared these isolates with nine reference isolates including the different subgroups in AG-3 (PT, TB and TM) and AG-2-Nt (pathogen of tobacco leaf spot) within AG-2-1 in terms of pathogenicity to tomato, tobacco and potato. All eight isolates caused foot rot on tomato. The six AG-3 isolates caused stem rot on young potato plants. While, all reference isolates of AG-3 PT causing stem rot of young potato plants incited foot rot on tomato. The two AG-2-1 isolates and an AG-2-Nt reference isolate caused severe leaf spot on tobacco leaves. The sequences of rDNA- ITS region and rDNA-IGS1 region of the AG-3 isolates showed high similarity to that of AG-3 PT isolates. Phylogenetic tree based on ITS and IGS1 regions of rDNA indicated that the AG-2-1 isolates from tomato formed a single clade with AG-2-Nt isolates and that they were separate from Japanese AG-2-1 isolates (culture type II). Pathogenicity tests and DNA sequence evaluation of the causal fungi revealed that the present isolates of AG-3 and AG-2-1 belonged to AG-3 PT and AG-2-Nt, respectively. This is the first report of tomato foot rot caused by R. solani in Japan.  相似文献   

14.
新疆加工型辣椒一种新的细菌性叶斑病病原的鉴定   总被引:1,自引:0,他引:1  
2014—2015年在新疆沙湾县加工型辣椒Capsicum annuumL.上发现一种细菌性叶斑病。为明确其病原种类,采用组织分离法分离病原菌,依据柯赫氏法则进行致病性测定,并对菌株进行16S rDNA和持家基因rpoD及gry B的扩增、序列测定和系统发育分析,对其进行鉴定。结果表明,获得的8个细菌菌株间致病力无明显差异。致病细菌与已报道的黄褐假单胞菌Pseudomonas fulva菌株的16S rDNA、rpoD基因、gry B基因的同源性分别达到了99.1%~99.9%、99.4%~99.5%和97.6%~100.0%。结合革兰氏染色反应、菌体形态、培养性状、生理生化反应、寄主范围等特征,将病原菌鉴定为黄褐假单胞菌。该病原菌通过人工接种还能侵染番茄、茄子、马铃薯、黄瓜、西瓜、甜瓜、四季豆、豆角、豇豆、白菜、萝卜、胡萝卜及芹菜等多种植物。  相似文献   

15.
Agave tequilana is the raw material for the production of the alcoholic beverage tequila. A bacterial disease has affected the A. tequilana crop in recent years. Previous reports based on colony and cell morphology, Gram stain and potato rot indicated that Erwinia sp. is the main pathogen. We isolated a several bacterial isolates capable of producing soft-rot symptoms in greenhouse pathogenicity assays. An extensive characterisation involving pathogenicity tests, fatty acid profile, metabolic and physiological properties, ribosomal DNA sequence and intergenic transcribed spacer amplification (ITS-PCR) and restriction banding pattern (ITS-RFLP) was made of each isolate. Three different species: Erwinia cacticida, Pantoea agglomerans and Pseudomonas sp. were identified. Fatty acid and metabolic profiles gave low similarity values of identification but 16S rDNA sequence, ITS-PCR and ITS-RFLP confirmed the identification of E. cacticida. In the phylogenetic tree, E. cacticida from blue agave was grouped neither with E. cacticida type strains nor with Erwinia carotovora. This is the first report that associates E. cacticida with A. tequilana soft-rot symptoms.  相似文献   

16.
The etiology of a new soft rot disease of tulips, causing leaf spots, leaf blight, neck and bulb rot in Konya, Turkey, was investigated. This disease occurred in tulip fields grown for seed bulbs of various varieties in 2002. Bacteria were isolated from the lesions on leaf, bud neck and bulbs and the causal bacterium was identified asPectobacterium carotovorum on the basis of biochemical and physiological tests. Cells were Gram-negative, rod-shaped, fermentative, potato-rot positive. Colonies were capable of growth at 37°C. On nutrient agar the colonies were creamy-white. The isolates were non-fluorescent on King’s B medium, positive for acetoin production, gelatin liquefaction, acid-production-from-lactose, and catalase; and negative for gas from glucose, reducing substances from sucrose, and phosphatase activity. Additionally, tests for egg yolk (lecithin), sensitivity to erythromycin, and pigmentation on yeast dextrose carbonate agar were negative; growth on 5% sodium chloride was positive. All the bacterial isolates obtained from the leaf, bud neck and bulbs produced the original symptoms following inoculation to the susceptible tulip variety ‘Gander’. The rate of damage caused by this bacterium was evaluated on several tulip varieties under field and storage conditions. Gander was the most susceptible variety in the field whereas ‘Salmon Parrot’ exhibited the highest rate of bulb rot in storage. Disease severity was lower in 2003 than 2002. http://www.phytoparasitica.org posting May 14, 2006.  相似文献   

17.
In 1995, Fusarium root rot of crisp head lettuce, caused by Fusarium oxysporum f. sp. lactucae, was simultaneously found in the Shiojiri and Kawakami areas of Nagano Prefecture, Japan. The Shiojiri and Kawakami isolates differed in pathogenicity to lettuce cultivars. Because of this distinct physiological specialization, these Shiojiri and Kawakami isolates should be designated as race 1 and race 2, respectively, using lines VP1010 (highly resistant to race 1), VP1013 (highly resistant to race 2) and variety Patriot (highly susceptible to both races) as differential varieties. This is the first report of races of Fusarium oxysporum f. sp. lactucae, Received 21 September 2000/ Accepted in revised form 21 March 2001  相似文献   

18.
In the present study, the pathogenicity of 36 isolates of Guignardia species isolated from asymptomatic ‘Tahiti’ acid lime fruit peels and leaves, ‘Pêra-Rio’ sweet orange leaves and fruit peel lesions, and a banana leaf were characterized. For pathogenicity testing, discs of citrus leaves colonized by Phyllosticta citricarpa under controlled laboratory conditions were kept in contact with the peels of fruit that were in susceptible states. In addition, pathogenicity was related to morphological characteristics of colonies on oatmeal (OA) and potato dextrose agar (PDA). This allowed the morphological differentiation between G. citricarpa and G. mangiferae. Polymerase chain reactions (PCRs) were also used to identify non-pathogenic isolates based on primers specific to G. citricarpa. A total of 14 pathogenic isolates were detected during pathogenicity tests. Five of these were obtained from leaf and fruit tissues of the ‘Tahiti’, which until this time had been considered resistant to the pathogen. Given that the G. citricarpa obtained from this host was pathogenic, it would be more appropriate to use the term insensitive rather than resistant to categorize G. citricarpa. A non-pathogenic isolate was obtained from lesions characteristic of citrus black spot (CBS), indicating that isolation of Guignardia spp. under these conditions does not necessarily imply isolation of pathogenic strains. This also applied to Guignardia spp. isolates from asymptomatic citrus tissues. Using fluorescent amplified fragment length polymorphism (fAFLP) markers, typically pathogenic isolates were shown to be more closely related to one another than to the non-pathogenic forms, indicating that the non-pathogenic isolates display higher levels of genetic diversity.  相似文献   

19.
安徽省大豆疫霉根腐病菌的鉴定及rDNA-ITS序列分析   总被引:1,自引:0,他引:1  
为明确安徽省夏大豆疫霉根腐病的病原菌种类,对采集自涡阳、怀远、固镇3个县的夏大豆病株及土样分离纯化后获得28株菌株,选取6株代表性菌株,通过形态学观察及核糖体DNA-ITS序列分析对其进行鉴定,并测定了其致病型。结果表明,6株菌株在利马豆培养基上菌落白色,质地均匀;菌丝无隔,致密,具近直角分枝;在10%V8C培养液中,游动孢子囊顶生,不脱落,卵形至椭圆形,无明显乳突,有内层出现象,长宽比大于1.6∶1;同宗配合,在利马豆培养基上单株培养产生大量卵孢子,藏卵器球形,雄器大多侧生;接种合丰35大豆品种后出现典型的大豆疫霉根腐病症状。r DNA-ITS序列分析表明,6株菌株与Gen Bank中大豆疫霉Phytophthora sojae的ITS序列同源性高达100%;菌株GY4、GY8、HY11、HY16、GZ10、GZ21的毒力公式分别为1b,2,3a,3b,4,5,6,7;1b,1d,3a,3b;1d,3a,3b,3c,4,5,6,7;2,3c,4,5,6,7;1b,3a,3c,5,8;3a,3b,5,6,7,8;属于6个不同的致病型。研究表明,这6株菌株均为大豆疫霉。  相似文献   

20.
Since 2011, the outbreaks of brown rot caused by Ralstonia solanacearum race 3, biovar 2, phylotype IIB-1 (R3/B2/PIIB-1) have significantly compromised potato production in Serbia. During 6 years of monitoring (2013–2018) among 3,524 potato tuber samples, 344 were found positive for brown rot disease. R. solanacearum R3/B2/PIIB-1 was isolated from seven cultivars among 12 monitored, and in five localities among 17 monitored. Cultivar Lady Claire was found to have the highest disease frequency (31.98%). A total of 78 isolates were identified by R. solanacearum-specific primer pairs (PS-1/PS-2 and OLI-1/Y-2), as well as the following tests: restriction fragment length polymorphism analysis, biovar determination, immunofluorescence, biochemical analysis, and pathogenicity. The genetic composition of 36 selected isolates assessed using multilocus sequence analysis with seven genes (adk, gapA, gdhA, gyrB, ppsA, hrpB, and fliC) showed that all isolates originating from Serbian potato were homogeneous. By using the TCS algorithm of concatenated sequences to get insight into the phylogeography of isolates and other R. solanacearum strains deposited in the NCBI database, we showed that their origin is undetermined. Peroxidase (POD) activity was measured in brown rotted potato tubers. A positive correlation was found between POD activity and disease severity rated on the analysed tubers. In general, POD activity increased by 2–22 times in vascular necrotic tissues compared to non-necrotic ones, and depended on disease severity but not on cultivar. Native polyacrylamide gel electrophoresis analysis of POD profiles resulted in a total of 10 distinct POD isoforms, of which PODs 3–5 were highly intensified in response to R. solanacearum.  相似文献   

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