Physiological Plant Pathology最新文献

筛选
英文 中文
Contents of volume 26 第二十六卷内容
Physiological Plant Pathology Pub Date : 1985-01-01 DOI: 10.1016/0048-4059(85)90079-7
{"title":"Contents of volume 26","authors":"","doi":"10.1016/0048-4059(85)90079-7","DOIUrl":"https://doi.org/10.1016/0048-4059(85)90079-7","url":null,"abstract":"","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"26 ","pages":"Pages iii-v"},"PeriodicalIF":0.0,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90079-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136926573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Index to volume 26 第26卷索引
Physiological Plant Pathology Pub Date : 1985-01-01 DOI: 10.1016/0048-4059(85)90080-3
{"title":"Index to volume 26","authors":"","doi":"10.1016/0048-4059(85)90080-3","DOIUrl":"https://doi.org/10.1016/0048-4059(85)90080-3","url":null,"abstract":"","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"26 ","pages":"Pages 389-396"},"PeriodicalIF":0.0,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90080-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136928872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tolerance of white bean (Phaseolus vulgaris) to white mold (Sclerotinia sclerotiorum) associated with tolerance to oxalic acid 白豆(Phaseolus vulgaris)对与草酸耐受性相关的菌核菌(Sclerotinia sclerotiorum)的耐受性
Physiological Plant Pathology Pub Date : 1985-01-01 DOI: 10.1016/0048-4059(85)90034-7
J.C. Tu
{"title":"Tolerance of white bean (Phaseolus vulgaris) to white mold (Sclerotinia sclerotiorum) associated with tolerance to oxalic acid","authors":"J.C. Tu","doi":"10.1016/0048-4059(85)90034-7","DOIUrl":"10.1016/0048-4059(85)90034-7","url":null,"abstract":"<div><p>The growth of <em>Sclerotinia sclerotiorum</em> in white beans (<em>Phaseolus vulgaris</em>) was much slower in the tolerant cv. Ex Rico-23 than in the susceptible cvs. Kentwood and Seafarer. The difference was paralleled by the rate of diffusion in leaf tissue of oxalic acid, a phytotoxin of the white mold fungus (<em>Sclerotinia sclerotiorum</em>). Uptake of oxalic acid into excised leaves through the petiole resulted in more severe brown-rot-like symptoms in the leaves of cv. Kentwood than in those of Ex Rico-23. When [<sup>14</sup>C] oxalic acid was fed through petioles, radioactivity in the interveinal tissue of Kentwood was about three times higher than that in Ex Rico-23. Autoradiographs of leaves showed that radioactivity in Ex Rico-23 was confined to major veins and that activity in the interveinal tissue was low, whereas in Seafarer and Kentwood radioactivity did not accumulate in the veins but was distributed uniformly throughout the leaf tissue, with a slight accumulation along leaf margins.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"26 1","pages":"Pages 111-117"},"PeriodicalIF":0.0,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90034-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84342726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 46
Photosynthesis 光合作用
Physiological Plant Pathology Pub Date : 1985-01-01 DOI: 10.1016/0048-4059(85)90037-2
C.M. Willmer
{"title":"Photosynthesis","authors":"C.M. Willmer","doi":"10.1016/0048-4059(85)90037-2","DOIUrl":"https://doi.org/10.1016/0048-4059(85)90037-2","url":null,"abstract":"","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"26 1","pages":"Pages 120-121"},"PeriodicalIF":0.0,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90037-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91981823","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Involvement of the phytoalexin medicarpin in the differential response of callus lines of lucerne (Medicago sativa) to infection by Verticillium albo-atrum 植物抗菌素与紫花苜蓿愈伤组织对黄萎病菌感染差异反应的关系
Physiological Plant Pathology Pub Date : 1985-01-01 DOI: 10.1016/0048-4059(85)90028-1
A.O. Latunde-Dada, J.A. Lucas
{"title":"Involvement of the phytoalexin medicarpin in the differential response of callus lines of lucerne (Medicago sativa) to infection by Verticillium albo-atrum","authors":"A.O. Latunde-Dada,&nbsp;J.A. Lucas","doi":"10.1016/0048-4059(85)90028-1","DOIUrl":"10.1016/0048-4059(85)90028-1","url":null,"abstract":"<div><p>Callus cultures derived from seeds of lucerne (<em>Medicago saliva</em> L.) were challenged with a lucerne isolate of <em>Verticillium albo-atrum</em> using agar blocks or spore suspensions as inoculum. The rate of colonization of different callus lines by the fungus varied from complete overgrowth of tissues in susceptible lines, to a rapid browning reaction of host cells accompanied by a restriction of fungal growth in resistant lines. The phytoalexin medicarpin accumulated in both resistant and susceptible reaction types, but resistant callus lines accumulated higher levels of this compound upon challenge with spore suspensions of <em>V. albo-atrum</em>. Pretreatment of resistant calli with subherbicidal levels of the inhibitor glyphosate lowered the production of medicarpin, reduced the browning response of callus cells and enhanced colonization by the fungus. Possible links between these <em>in vitro</em> responses and those of intact lucerne plants to <em>V. albo-atrum</em> are discussed.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"26 1","pages":"Pages 31-42"},"PeriodicalIF":0.0,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(85)90028-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83790469","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 43
Characterization of the parasitic interface between Erysiphe pisi and Pisum sativum using fluorescent probes 用荧光探针研究猪刺槐与猪刺槐寄生界面
Physiological Plant Pathology Pub Date : 1984-11-01 DOI: 10.1016/0048-4059(84)90035-3
J.M. Chard , J.L. Gay
{"title":"Characterization of the parasitic interface between Erysiphe pisi and Pisum sativum using fluorescent probes","authors":"J.M. Chard ,&nbsp;J.L. Gay","doi":"10.1016/0048-4059(84)90035-3","DOIUrl":"10.1016/0048-4059(84)90035-3","url":null,"abstract":"<div><p>The constituents of the interface between a strain of <em>Erysiphe pisi</em>and two susceptible and five resistant lines of <em>Pisum sativum</em> were investigated by fluorescence microscopy after treatment with specific reagents. Fragments of epidermes were detached so that the haustoria and extrahaustorial membranes were exposed directly to the reagents. The specificities of the 23 reagents employed included α- and β-linkages in polysaccharides; constituent sugars; aldehyde, amino, sulphydryl and disulphide groups; proteins, lysine, arginine, lipid, calcium and anions; and anion transport sites.</p><p>The main conclusions are that in the susceptible cultivars the extrahaustorial membrane includes polysaccharides (β1–4 linked) with small amounts of α-glucose, α-mannose and galactose, β-linked N-acetylglucosamine (haustorial face only), protein, arginine, amino and sulphydryl groups and calcium. The extrahaustorial matrix includes varying quantities of β-linked polysaccharides. Haustorial walls contain β-linked polysaccharides including α-glucose, α-mannose, galactose and N-acetyl glucosamine (β-linked). The haustorial cytoplasm contains protein and releases fluorescein from fluorescein diacetate and 3-<em>o</em>-methyl fluorescein phosphate.</p><p>The main differences between the susceptible lines and the resistant lines is that the resistant line, show enhanced reactivity of terminal glucose, mannose and N-acetylglucosamine groups in the extrahaustorial membranes of some lines. The last is probably due to greater accessibility of lectin effected by rupture of extrahaustorial membranes. Constituents of extrahaustorial membranes fluorescing with 4-acetamido-4′-<em>iso</em>-thiocyanato-stilbene-2,2′-disulphonic acid developed ore slowly and included less cross-linked protein. Calcium was rare in the extrahaustorial membranes and host cytoplasm in resistant lines.</p><p>The results are discussed in relation to the molecular and functional properties of the interface.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 259-276"},"PeriodicalIF":0.0,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90035-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78091328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
The role of papillae in resistance to powdery mildew conditioned by the ml-o gene in barley. II. Experimental evidence 大麦乳突在ml-o基因调控下抗白粉病的作用。2实验证据
Physiological Plant Pathology Pub Date : 1984-11-01 DOI: 10.1016/0048-4059(84)90042-0
Mark C. Stolzenburg, James R. Aist, Herbert W. Israel
{"title":"The role of papillae in resistance to powdery mildew conditioned by the ml-o gene in barley. II. Experimental evidence","authors":"Mark C. Stolzenburg,&nbsp;James R. Aist,&nbsp;Herbert W. Israel","doi":"10.1016/0048-4059(84)90042-0","DOIUrl":"10.1016/0048-4059(84)90042-0","url":null,"abstract":"<div><p>The <em>ml-o</em> gene in barley conditions resistance to primary penetration by <em>Erysiphe graminis</em> f. sp. <em>hordei</em> as well as an enhanced papilla response. To determine if papillae are necessary for <em>ml-o</em> resistance, cytoplasmic aggregation and papilla formation Were inhibited in near-isogenic resistant-susceptible pairs of barley breeding lines by low-speed centrifugation of leaves and centrifugation and heat-shock treatments of coleoptiles. Papilla frequency was markedly reduced by both methods. Centrifugation separated papilla formation from resistance at most encounter sites, although a small increase in penetration efficiency occurred because haustoria developed at some sites where papilla formation was inhibited. Heat-shock caused a substantial increase in penetration efficiency. Here too, this increase occurred because haustoria developed at sites where papilla formation was inhibited. Taken together, these results demonstrate a strong link between papilla formation and <em>ml-o</em> resistance, but they do not uniformly support the hypothesis that <em>ml-o</em> resistance is based on papilla formation. The centrifugation results, in particular, suggest that papilla formation is not necessary for resistance.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 347-361"},"PeriodicalIF":0.0,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90042-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87447490","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 27
Subcellular localization by immunocytochemistry of the extracellular protease produced by Nectria galligena Bres. in infected apple tissue 利用免疫细胞化学方法对高脂血菌胞外蛋白酶进行亚细胞定位。在感染的苹果组织中
Physiological Plant Pathology Pub Date : 1984-11-01 DOI: 10.1016/0048-4059(84)90040-7
M.E.C. Rey , J.P. Noble
{"title":"Subcellular localization by immunocytochemistry of the extracellular protease produced by Nectria galligena Bres. in infected apple tissue","authors":"M.E.C. Rey ,&nbsp;J.P. Noble","doi":"10.1016/0048-4059(84)90040-7","DOIUrl":"10.1016/0048-4059(84)90040-7","url":null,"abstract":"<div><p>Existing evidence implicates an extracellular protease of <em>Nectria galligena</em> Bres. in the initiation of the accumulation of antifungal amounts of benzoic acid in immature apple fruit. It is the purpose of the present work to examine further this relationship between protease and the host cells by immunocytochemical techniques.</p><p>Thin sections of infected apple tissue, fixed, and embedded in Lowicryl K4M at −40°C were reacted with monospecific antibodies raised in rabbits against the purified protease. Using a secondary tetramethylrhodamine isothiocyanate conjugated antibody, specific fluorescent localization of intercellular and intracellular fungal hyphae and host cell cytoplasm was demonstrated, thus establishing the presence of the protease in infected tissue. In a transmission electron microscope study, this was confirmed, and the localization and distribution of the enzyme further resolved by protein A-gold immunocytochemistry. Specific binding of colloidal gold was evident over, (1) intercellular and intracellular fungal hyphae, (2) electron-dense deposits located within and around hyphae and adjacent to partially degraded apple cell walls, and (3) peripheral vacuolar cytoplasm of intact host cells. These observations suggest that protease synthesized in hyphae of <em>N. galligena</em> is secreted into an extracellular matrix whence it may diffuse through host cell walls and detached, but entire, plasmalemmae observed in infected tissues. The protease is, therefore, able to reach sites in the host where it may elicit benzoic acid or where it may release an endogenous elicitor for that purpose. This is essential supporting evidence for the hypothesis that the accumulation of benzoic acid is initiated by fungal protease <em>in vivo</em>.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 323-336"},"PeriodicalIF":0.0,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90040-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78178511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Production and metabolism of 6-methoxymellein in cultured carrot cells 胡萝卜细胞中6-甲氧基甲基lein的产生和代谢
Physiological Plant Pathology Pub Date : 1984-11-01 DOI: 10.1016/0048-4059(84)90039-0
Fumiya Kurosaki, Kimiko Matsui, Arasuke Nishi
{"title":"Production and metabolism of 6-methoxymellein in cultured carrot cells","authors":"Fumiya Kurosaki,&nbsp;Kimiko Matsui,&nbsp;Arasuke Nishi","doi":"10.1016/0048-4059(84)90039-0","DOIUrl":"10.1016/0048-4059(84)90039-0","url":null,"abstract":"<div><p>The carrot phytoalexin, 6-methoxymellein, accumulated in carrot suspension culture when it was incubated with a partial hydrolysate of carrot cells obtained by pectinase or trypsin treatment. 6-Methoxymellein also accumulated when these enzymes were added to the culture. In both cases, phytoalexin content decreased rapidly after maximum accumulation was attained, suggesting that the cultured carrot cells metabolized the phytoalexin.</p><p>Cultured carrot cells incubated with the phytoalexin formed three different metabolites: among them, two which accumulated in the medium, were identified as the β-glucoside of 6-methoxymellein and 6-hydroxymellein.</p><p>6-Methoxymellein was found to be toxic to the host plant and induced a lag period in the growth of cultured carrot cells at low concentration. When it was added at concentrations higher than 0·5 m<span>m</span>, it caused a rapid decrease in viable cell number.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 313-322"},"PeriodicalIF":0.0,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90039-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85368860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 44
Distribution of Odontoglossum ringspot virus in apical meristems of infected Cymbidium cultivars 牙舌环斑病毒在染病大花蕙兰品种顶端分生组织中的分布
Physiological Plant Pathology Pub Date : 1984-11-01 DOI: 10.1016/0048-4059(84)90037-7
A. Toussaint , D. Dekegel, G. Vanheule
{"title":"Distribution of Odontoglossum ringspot virus in apical meristems of infected Cymbidium cultivars","authors":"A. Toussaint ,&nbsp;D. Dekegel,&nbsp;G. Vanheule","doi":"10.1016/0048-4059(84)90037-7","DOIUrl":"10.1016/0048-4059(84)90037-7","url":null,"abstract":"<div><p>The presence of <em>Odontoglossum</em> ringspot virus in the lateral and apical meristem domes of <em>Cymbidium</em> cultivars was revealed by electron microscopy. The analysis of transverse serial ultra-thin sections of apical meristems and of longitudinal serial ultra-thin sections of axillary bud meristems of donor plants, and of apical meristems of plantlets cultured from excised meristems, confirmed the presence of virus in the meristematic regions.</p><p>These observations provide an explanation for the difficulties encountered in obtaining virus-free <em>Cymbidium</em> cv plantlets by meristem culture.</p></div>","PeriodicalId":101028,"journal":{"name":"Physiological Plant Pathology","volume":"25 3","pages":"Pages 297-305"},"PeriodicalIF":0.0,"publicationDate":"1984-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0048-4059(84)90037-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75987755","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信