1970
DOI: 10.1017/s0024282970000427
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Physiological Aspects of Symbiotic Associations between Fungi and other Plants

D. H. Lewis
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1972
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Cited by 8 publications
(6 citation statements)
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“…Although other fractions into which photosynthate may be partitioned are not included in the present study, cucumber leaves in early stages of infection by S. fuliginea have previously been shown to incorporate twice as high a proportion of 14 C-labelled photosynthate into both storage and membrane lipids as healthy leaves (Abood & Lösel, 1989;Abood et al, 1990). Thus in this system, as with other biotrophic fungal pathogens, conversion of photosynthate to fungal polyols, trehalose, glycogen (Lewis, 1970;Long et al, 1975), lipid and other fungal constituents facilitates a high rate of transport across the host-pathogen interface to support the growth and sporulation of the mycelium.…”
Section: Discussionmentioning
confidence: 98%
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“…Although other fractions into which photosynthate may be partitioned are not included in the present study, cucumber leaves in early stages of infection by S. fuliginea have previously been shown to incorporate twice as high a proportion of 14 C-labelled photosynthate into both storage and membrane lipids as healthy leaves (Abood & Lösel, 1989;Abood et al, 1990). Thus in this system, as with other biotrophic fungal pathogens, conversion of photosynthate to fungal polyols, trehalose, glycogen (Lewis, 1970;Long et al, 1975), lipid and other fungal constituents facilitates a high rate of transport across the host-pathogen interface to support the growth and sporulation of the mycelium.…”
Section: Discussionmentioning
confidence: 98%
“…The substantial synthesis of polyols and trehalose, all virtually absent from healthy leaves, during the development of S. fuliginea in cucumber, is consistent with previous observations on powdery mildew infection of leaves of barley (Edwards & Allen, 1966); oak (Hewitt & Ayres, 1976); pea (Manners & Gay, 1982); and grapevine (Brem et al, 1986), although the relative proportions of individual fractions sometimes differed. As in other biotrophic infections, polyols provide the fungal partner with a a substantial mobile sink of reduced carbon, which is not normally accessible to host metabolism (Lewis & Smith, 1967;Lewis, 1970;Holligan et al, 1973;Holligan et al, 1974). The early acceleration of α-glucan synthesis immediately after inoculation, and its further dramatic rise between 5 and 7 dai, with marked alterations in the proportions of fractions of differing solubility, indicated rapid incorporation of photosynthate into fungal glucans, particularly glycogen, which then increased more slowly to a final value close to that attained by total glucans in healthy leaves.…”
Section: Discussionmentioning
confidence: 99%
“…A feature of the transfer of sucrose from host to parasite appears to be its hydrolysis before absorption (Yuen, 1969;Lewis, 1970). This is supported by the absolute increase in amount of hexoses in infected regions of Tussilago and the increased incorporation of radioactivity into them (Table 3).…”
Section: Discussionmentioning
confidence: 98%
“…Las Ericáceas parecen tener su origen en el temprano Terciario (Lewis, 1987). Géneros como Arctostaphylos, Calluna, Erica, Rhododendron, Vaccinum, Epacris y Astroloma (Cairney & Ashford, 2002;Wang & Qiu, 2006) entre otros, han desarrollado un particular tipo de micorriza "ericoide" (Smith & Read, 2008) con Rhizoscyphus (Hymenoscyphus) ericae, cuya capacidad de formar simbiosis con hepáticas (Pressel & al., 2008) y ectomicorrizas con angiospermas y gimnospermas (Vrälstad & al., 2002) ha sido demostrada.…”
Section: De Los Cambios Del Terciario Al Cuaternario: Otros Tipos De unclassified