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牡丹根腐病原菌拮抗细菌抑菌活性物质分析 被引量:4
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作者 杨瑞先 刘萍 +2 位作者 王祖华 阮宝硕 汪智达 《生物技术通报》 CAS CSCD 北大核心 2022年第2期57-66,共10页
前期研究发现解淀粉芽胞杆菌(Bacillus amyloliquefaciens)md8和md9对牡丹根腐病原菌具有较好的抑制作用,但其抑菌物质的组成尚不清楚。本文首先明确了2个菌株3种脂肽类物质合成的基因片段,利用酸沉淀和葡聚糖凝胶层析法进行抑菌物质的... 前期研究发现解淀粉芽胞杆菌(Bacillus amyloliquefaciens)md8和md9对牡丹根腐病原菌具有较好的抑制作用,但其抑菌物质的组成尚不清楚。本文首先明确了2个菌株3种脂肽类物质合成的基因片段,利用酸沉淀和葡聚糖凝胶层析法进行抑菌物质的分离纯化,牛津杯对峙法检测脂肽类粗提物和凝胶层析分离组分的抑菌活性;进一步利用实时荧光定量PCR(RT-qPCR)检测菌株在拮抗根腐病原菌过程中脂肽类物质合成基因相对表达量的变化,基质辅助激光解吸飞行时间质谱(MALDI-TOF-MS)分析抑菌物质的种类。结果表明,2个菌株的脂肽类粗提物和凝胶层析分离组分对根腐病原菌均具有良好的平板抑菌效果,RT-qPCR结果表明2个菌株合成伊枯草菌素(iturin)的基因ituD在对峙培养过程中相对表达量显著增加,芬荠素(fengycin)合成基因fenA也呈现上调表达。MALDI-TOF-MS分析表明2个菌株中具有抑菌作用的分离组分主要为伊枯草菌素类物质Iturin B和Bacillomycins D,结合实时荧光定量PCR结果,推测菌株md8和md9在拮抗根腐病原菌过程中发挥主要生防作用的物质为伊枯草菌素。 展开更多
关键词 牡丹 根腐病原菌 解淀粉芽胞杆菌 脂肽类物质合成基因 抑菌活性物质
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嫁接辣椒根系分泌物对根腐病和青枯病的影响 被引量:15
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作者 段曦 孙晨晨 +4 位作者 孙胜楠 吴帼秀 王洪涛 毕焕改 艾希珍 《园艺学报》 CAS CSCD 北大核心 2017年第2期297-306,共10页
采用浸根法收集辣椒根系分泌物,利用气相色谱—质谱技术(GC–MS)分析其化学组成,研究嫁接辣椒根系分泌物对辣椒根腐病和青枯病病原菌的化感作用。结果表明,砧木、嫁接辣椒和自根辣椒根系分泌物的组分存在较大差异,与自根辣椒根系分泌物... 采用浸根法收集辣椒根系分泌物,利用气相色谱—质谱技术(GC–MS)分析其化学组成,研究嫁接辣椒根系分泌物对辣椒根腐病和青枯病病原菌的化感作用。结果表明,砧木、嫁接辣椒和自根辣椒根系分泌物的组分存在较大差异,与自根辣椒根系分泌物相比,砧木和嫁接辣椒的根系分泌物能够抑制根腐病原菌腐皮镰孢菌(Fusarium solani)和青枯病原菌假单胞杆菌(Ralstonia solanacearum)的生长。表明嫁接辣椒根系分泌物组分变化是其减轻土传病害的重要机理之一。通过对砧木、嫁接和自根辣椒根系分泌物组分分析,推测砧木和嫁接辣椒根系分泌物中邻苯二甲酸二异辛酯和二苯并呋喃对病原菌生长起抑制作用,经功能鉴定证明,0.2 m L·L^(-1)的邻苯二甲酸二异辛酯和0.1 g·L^(-1)的二苯并呋喃可降低辣椒发病率,产量分别比对照(清水)高31.7%和38.3%。 展开更多
关键词 辣椒 嫁接 系分泌物 根腐病原菌 青枯病原菌
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Studies on the Isolation, Identification and In Vitro Growth Rates of the Three Pathogenic Fungi from Panax notoginseng Cultivated in Wenshan Eparchy 被引量:2
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作者 王文亚 赵昶灵 +5 位作者 陈中坚 文国松 魏富刚 龙廷菊 李孙文 王崇德 《Agricultural Science & Technology》 CAS 2015年第6期1165-1171,1258,共8页
Objective] The aim of this study was to simultaneously isolate and identify the main pathogenic fungi of the root rot, black spot and round spot from the Panax notoginseng plants cultivated in Wenshan Eparchy of Yunna... Objective] The aim of this study was to simultaneously isolate and identify the main pathogenic fungi of the root rot, black spot and round spot from the Panax notoginseng plants cultivated in Wenshan Eparchy of Yunnan Province of China. [Method] The pathogenic fungi were isolated and purified by using potato dextrose agar (PDA) medium. The morphological identification was accomplished first according to the colony forms of the fungi when cultivated in vitro, then accord-ing to the symptom characteristics and colony forms of the re-isolated fungi in the reverse inoculation experiments. The molecular identification was performed accord-ing to the amplification and alignment of the internal transcribed space (ITS) se-quences of the fungi. The increases of the diameters and thickness of the colonies of the fungi cultivated in vitro were employed to indicate the growth rates of the fungi. [Results] The consistency of the colony forms and symptom characteristics and the 96%-99% similarities revealed in the ITS sequence alignments al proved that the main pathogenic fungi of the root rot, black spot and round spot of the P. notoginseng plants raised in Wenshan were Cylindrocarpon didymium, Alternaria panax and Mycocentrospora acerina, respectively. When cultivated in vitro in the same temperature, humidity and il umination, the increases of the colony diameters and thickness of C. didymium were the highest, fol owed by those of A. panax, then those of M. acerina. During different cultivation periods, the differences of the colony diameters and thickness of the three fungi al reached extremely significant level. However, at the same cultivation time, the differences of the diameters and thickness among the three fungi only reached significant level. [Conclusion] The main pathogenic fungi which result in the root rot, black spot and round spot of the P. notoginseng in Wenshan are C. didymium, A. panax and M. acerina, respec-tively. When these three diseases break out at the same time, the root rot wil spread fastest, fol owed orderly by the black spot and the round spot. 展开更多
关键词 Panax notoginseng cultivated in Wenshan Eparchy Root rot black spot and round spot Pathogenic fungus Growth rate in vitro
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Transient silencing mediated by in vitro synthesized double-stranded RNA indicates that PsCdc14 is required for sporangial development in a soybean root rot pathogen 被引量:3
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作者 ZHAO Wei YANG XinYu +3 位作者 DONG SuoMeng SHENG YuTing WANG YuanChao ZHENG XiaoBo 《Science China(Life Sciences)》 SCIE CAS 2011年第12期1143-1150,共8页
In many eukaryotic organisms, Cdcl4 phosphatase regulates multiple biological events during anaphase and is essential for mitosis. It has been shown that Cdcl4 is required for sporulation in the potato blight pathogen... In many eukaryotic organisms, Cdcl4 phosphatase regulates multiple biological events during anaphase and is essential for mitosis. It has been shown that Cdcl4 is required for sporulation in the potato blight pathogen Phytophthora infestans; howev- er, the role that the Cdcl4 homolog (PsCdcl4) plays in the soil-borne soybean root rot pathogen P. sojae remains ambiguous. PsCdc14 is highly expressed in spornlation, zoospore, and cyst life stages, but not in vegetative mycelia and infection stages, suggesting that it contributes to asexual reproduction and thus the spread of the disease. Double-stranded RNA (dsRNA) medi- ates gene silencing, a post-transcriptional and highly conserved process in eukaryotes, involving specific gene silencing through degradation of target mRNA. We combined in vitro dsRNA synthesis and a polyethylene glycol-mediated transfor- marion system to construct a dsRNA-mediated transient gene silencing system; and then performed a functional analysis of PsCdcl4 in P. sojae. PsCdc14 mRNA was dramatically reduced in transformants after protoplasts were exposed in in vitro synthesized PsCdc14 dsRNA, resulting in low sporangial production and abnormal development in P. sojae silencing lines. Furthermore, dsRNA-mediated transient gene silencing could enable elucidation of P. sojae rapid gene function, facilitating our understanding of the development and pathogenicity mechanisms of this oomycete fungus. 展开更多
关键词 Phytophthora sojae PsCdc14 sporangium transient gene silencing
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