The Glyoxylate Cycle in an Arbuscular Mycorrhizal Fungus. Carbon Flux and Gene Expression
Author(s) -
Peter J. Lammers,
Jeongwon Jun,
Jehad Abubaker,
Raul Arreola,
Anjali Gopalan,
Berta Bago,
Cinta Hernández-Sebastià,
James W. Allen,
David D. Douds,
Philip E. Pfeffer,
Yair ShacharHill
Publication year - 2001
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.010375
Subject(s) - glyoxylate cycle , isocitrate lyase , malate synthase , biology , spore germination , fungus , symbiosis , spore , germination , mycelium , biochemistry , mycorrhiza , botany , complementary dna , gene , enzyme , bacteria , genetics
The arbuscular mycorrhizal (AM) symbiosis is responsible for huge fluxes of photosynthetically fixed carbon from plants to the soil. Lipid, which is the dominant form of stored carbon in the fungal partner and which fuels spore germination, is made by the fungus within the root and is exported to the extraradical mycelium. We tested the hypothesis that the glyoxylate cycle is central to the flow of carbon in the AM symbiosis. The results of (13)C labeling of germinating spores and extraradical mycelium with (13)C(2)-acetate and (13)C(2)-glycerol and analysis by nuclear magnetic resonance spectroscopy indicate that there are very substantial fluxes through the glyoxylate cycle in the fungal partner. Full-length sequences obtained by polymerase chain reaction from a cDNA library from germinating spores of the AM fungus Glomus intraradices showed strong homology to gene sequences for isocitrate lyase and malate synthase from plants and other fungal species. Quantitative real-time polymerase chain reaction measurements show that these genes are expressed at significant levels during the symbiosis. Glyoxysome-like bodies were observed by electron microscopy in fungal structures where the glyoxylate cycle is expected to be active, which is consistent with the presence in both enzyme sequences of motifs associated with glyoxysomal targeting. We also identified among several hundred expressed sequence tags several enzymes of primary metabolism whose expression during spore germination is consistent with previous labeling studies and with fluxes into and out of the glyoxylate cycle.
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