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GintAMT3-a Low-Affinity Ammonium Transporter of the Arbuscular Mycorrhizal Rhizophagus irregularis
被引:46
作者:
Calabrese, Silvia
[1
]
Perez-Tienda, Jacob
[2
]
Ellerbeck, Matthias
[3
]
Arnould, Christine
[4
]
Chatagnier, Odile
[4
]
Boller, Thomas
[1
]
Schuessler, Arthur
Brachmann, Andreas
[3
]
Wipf, Daniel
[4
]
Ferrol, Nuria
[2
]
Courty, Pierre-Emmanuel
[1
]
机构:
[1] Univ Basel, Dept Environm Sci, Bot, Zurich Basel Plant Sci Ctr, Basel, Switzerland
[2] CSIC, Estn Expt Zaidin, Dept Microbiol Suelo & Sistemas Simbiot, Granada, Spain
[3] Univ Munich, Fac Biol, Genet, Planegg Martinsried, Germany
[4] Univ Bourgogne Franche Comte, INRA, CNRS, Agroecol,AgroSup Dijon, Dijon, France
基金:
美国国家科学基金会;
关键词:
arbuscular mycorrhizal fungi;
ammonium transporter;
low affinity transporter;
extraradical mycelium;
intraradical mycelium;
FUNGUS GLOMUS-INTRARADICES;
NITROGEN TRANSFER;
RICE ROOTS;
IN-VITRO;
MOLECULAR CHARACTERIZATION;
HYPHAL GROWTH;
EXPRESSION;
FAMILY;
METABOLISM;
MEMBRANE;
D O I:
10.3389/fpls.2016.00679
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Nutrient acquisition and transfer are essential steps in the arbuscular mycorrhizal (AM) symbiosis, which is formed by the majority of land plants. Mineral nutrients are taken up by AM fungi from the soil and transferred to the plant partner. Within the cortical plant root cells the fungal hyphae form tree-like structures (arbuscules) where the nutrients are released to the plant-fungal interface, i.e., to the periarbuscular space, before being taken up by the plant. In exchange, the AM fungi receive carbohydrates from the plant host. Besides the well studied uptake of phosphorus (P), the uptake and transfer of nitrogen (N) plays a crucial role in this mutualistic interaction. In the AM fungus Rhizophagus irregularis (formerly called Glomus intraradices), two ammonium transporters (AMT) were previously described, namely GintAMT1 and GintAMT2. Here, we report the identification and characterization of a newly identified R. irregularis AMT, GintAMT3. Phylogenetic analyses revealed high sequence similarity to previously identified AM fungal AMTs and a clear separation from other fungal AMTs. Topological analysis indicated GintAMT3 to be a membrane bound pore forming protein, and GFP tagging showed it to be highly expressed in the intraradical mycelium of a fully established AM symbiosis. Expression of GintAMT3 in yeast successfully complemented the yeast AMT triple deletion mutant (MATa ura3 mep1 Delta mep2 Delta::LEU2 mep3 Delta::KanMX2). GintAMT3 is characterized as a low affinity transport system with an apparent K-m of 1.8 mM and a V-max of 240 nmol(-1) min(-1) 10(8) cells(-1), which is regulated by substrate concentration and carbon supply.
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