The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Carbon Uptake and the Metabolism and Transport of Lipids in an Arbuscular Mycorrhiza1
Open accessAbstract
Both the plant and the fungus benefit nutritionally in the arbuscular mycorrhizal symbiosis: The host plant enjoys enhanced mineral uptake and the fungus receives fixed carbon. In this exchange the uptake, metabolism, and translocation of carbon by the fungal partner are poorly understood. We therefore analyzed the fate of isotopically labeled substrates in an arbuscular mycorrhiza (in vitro cultures of Ri T-DNA-transformed carrot [Daucus carota] roots colonized by Glomus intraradices) using nuclear magnetic resonance spectroscopy. Labeling patterns observed in lipids and carbohydrates after substrates were supplied to the mycorrhizal roots or the extraradical mycelium indicated that: (a)13C-labeled glucose and fructose (but not mannitol or succinate) are effectively taken up by the fungus within the root and are metabolized to yield labeled carbohydrates and lipids; (b) the extraradical mycelium does not use exogenous sugars for catabolism, storage, or transfer to the host; (c) the fungus converts sugars taken up in the root compartment into lipids that are then translocated to the extraradical mycelium (there being little or no lipid synthesis in the external mycelium); and (d) hexose in fungal tissue undergoes substantially higher fluxes through an oxidative pentose phosphate pathway than does hexose in the host plant.
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Phillips, J. M., & Hayman, D. S. (1970) · Transactions of the British Mycological Society · doi:10.1016/s0007-1536(70)80110-3 · Cited by 8,495
(2008) · Elsevier eBooks · doi:10.1016/b978-0-12-370526-6.x5001-6 · Cited by 7,431
Smith, S. E., Read, D. J., & Harley, J. L. (1997) · Cited by 1,243
Net transfer of carbon between ectomycorrhizal tree species in the field
Simard, S. W., Perry, D. A., Jones, M. D., Myrold, D. D., Durall, D. M., & Molina, R. (1997) · Nature · doi:10.1038/41557 · Cited by 1,053
Boreal forest plants take up organic nitrogen
Näsholm, T., Ekblad, A., Nordin, A., Giesler, R., Högberg, M., & Högberg, P. (1998) · Nature · doi:10.1038/31921 · Cited by 1,030
Early events of vesicular–arbuscular mycorrhiza formation on Ri T‐DNA transformed roots
BÉCARD, G., & FORTIN, J. A. (1988) · New Phytologist · doi:10.1111/j.1469-8137.1988.tb03698.x · Cited by 862
Advances in the Study of Vesicular-Arbuscular Mycorrhiza
Mosse, B. (1973) · Annual Review of Phytopathology · doi:10.1146/annurev.py.11.090173.001131 · Cited by 654
Regulation of trehalose mobilization in fungi
Thevelein, J. M. (1984) · Microbiological Reviews · doi:10.1128/mmbr.48.1.42-59.1984 · Cited by 565
The Shikimate Pathway as an Entry to Aromatic Secondary Metabolism
Herrmann, K. M. (1995) · Plant Physiology · doi:10.1104/pp.107.1.7 · Cited by 462
(1996) · Springer eBooks · doi:10.1007/978-1-4613-1213-0 · Cited by 426
Role of Arbuscular Mycorrhizal Fungi in Uptake of Phosphorus and Nitrogen From Soil
George, E., Marschner, H., & Jakobsen, I. (1995) · Critical Reviews in Biotechnology · doi:10.3109/07388559509147412 · Cited by 383
Heat-induced accumulation and futile cycling of trehalose in Saccharomyces cerevisiae
Hottiger, T., Schmutz, P., & Wiemken, A. (1987) · Journal of Bacteriology · doi:10.1128/jb.169.12.5518-5522.1987 · Cited by 284
Fatty acids. Part 50. 13C nuclear magnetic resonance studies of olefinic fatty acids and esters
Gunstone, F. D., Pollard, M. R., Scrimgeour, C. M., & Vedanayagam, H. S. (1977) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(77)90031-7 · Cited by 242
Fatty Acid methyl ester profiles for characterization of glomalean fungi and their endomycorrhizae
Graham, J. H., Hodge, N. C., & Morton, J. B. (1995) · Applied and Environmental Microbiology · doi:10.1128/aem.61.1.58-64.1995 · Cited by 233
Trehalose and trehalase in plants: recent developments
Müller, J., Boller, T., & Wiemken, A. (1995) · Plant Science · doi:10.1016/0168-9452(95)04218-j · Cited by 210
Use of sugars by intraradical hyphae of arbuscular mycorrhizal fungi revealed by radiorespirometry
SOLAIMANAND, M. Z., & SAITO, M. (1997) · New Phytologist · doi:10.1046/j.1469-8137.1997.00757.x · Cited by 185
Dieuaide-Noubhani, M., Raffard, G., Canioni, P., Pradet, A., & Raymond, P. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.22.13147 · Cited by 166
Biocontrol of plant pathogens using arbuscular mycorrhizal fungi
Hooker, J. E., Jaizme-Vega, M. C., & Atkinson, D. (1994) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8504-1_15 · Cited by 141
13C labeling in studies of metabolic regulation
London, R. E. (1988) · Progress in Nuclear Magnetic Resonance Spectroscopy · doi:10.1016/0079-6565(88)80010-4 · Cited by 139
In Vivo31P NMR Studies of Corn Root Tissue and Its Uptake of Toxic Metals
Pfeffer, P. E., Tu, S.-I., Gerasimowicz, W. V., & Cavanaugh, J. R. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.80.1.77 · Cited by 127
Self-citationAn overwintering cover crop increases inoculum of VAM fungi in agricultural soil
Galvez, L., Douds, D. D., Wagoner, P., et al. (1995) · Renewable Agriculture and Food Systems · doi:10.1017/s0889189300006391 · Cited by 103
Self-citationBécard, G., Doner, L. W., Rolin, D., Douds, D. D., & PFEFFER, P. E. (1991) · New Phytologist · doi:10.1111/j.1469-8137.1991.tb00994.x · Cited by 86
Self-citationCompatible solutes – the mycological dimension and their role as physiological buffering agents
Jennings, D. H., & BURKE, R. M. (1990) · New Phytologist · doi:10.1111/j.1469-8137.1990.tb04715.x · Cited by 77
Occurrence of trehalose in vesicular-arbuscular mycorrhizal fungi and in mycorrhizal roots
Schubert, A., Wyss, P., & Wiemken, A. (1992) · Journal of Plant Physiology · doi:10.1016/s0176-1617(11)81054-0 · Cited by 67
Cited by
Nitrogen transfer in the arbuscular mycorrhizal symbiosis
Govindarajulu, M., Pfeffer, P. E., Jin, H., Abubaker, J., Douds, D. D., Allen, J. W., Bücking, H., Lammers, P. J., & Shachar-Hill, Y. (2005) · Nature · doi:10.1038/nature03610 · Cited by 1,068
Self-citationCarbon Metabolism and Transport in Arbuscular Mycorrhizas
Bago, B., Pfeffer, P. E., & Shachar-Hill, Y. (2000) · Plant Physiology · doi:10.1104/pp.124.3.949 · Cited by 600
Self-citationLipid transfer from plants to arbuscular mycorrhiza fungi
Keymer, A., Pimprikar, P., Wewer, V., Huber, C., Brands, M., Bucerius, S. L., Delaux, P.-M., Klingl, V., Röpenack-Lahaye, E. V., Wang, T. L., et al. (2017) · eLife · doi:10.7554/elife.29107 · Cited by 465
Mycorrhizal networks: a review of their extent, function, and importance
Simard, S. W., & Durall, D. M. (2004) · Canadian Journal of Botany · doi:10.1139/b04-116 · Cited by 443
Fellbaum, C. R., Gachomo, E. W., Beesetty, Y., Choudhari, S., Strahan, G. D., Pfeffer, P. E., Kiers, E. T., & Bücking, H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118650109 · Cited by 425
Self-citation
Metadata
- Authors
- Pfeffer, P. E., Douds, D. D., Bécard, G., & Shachar-Hill, Y.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 1999-06-01
- Volume
- 120
- Issue
- 2
- Pages
- 587-598
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W1977525920
- Cited by
- 403
- References
- 24
- FWCI
- 22.10
- Type
- journal article
- Language
- en
- Open access
- bronze
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