A re-assessment of sucrose signaling involved in cluster-root formation and function in phosphate-deficient white lupin (Lupinus albus)

被引:19
|
作者
Wang, Zhengrui [1 ]
Shen, Jianbo [2 ]
Ludewig, Uwe [1 ]
Neumann, Guenter [1 ]
机构
[1] Univ Hohenheim, Inst Crop Sci, Nutr Crop Physiol 340h, D-70593 Stuttgart, Germany
[2] China Agr Univ, Dept Plant Nutr, Key Lab Plant Soil Interact, Beijing 100193, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
STIMULATE ETHYLENE PRODUCTION; INDUCED GENE-EXPRESSION; TOBACCO LEAF-DISKS; PHOSPHORUS-DEFICIENCY; CITRATE EXUDATION; PROTEOID ROOTS; ENHANCED EXPRESSION; SYSTEM ARCHITECTURE; ACID EXCRETION; NITRIC-OXIDE;
D O I
10.1111/ppl.12311
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Apart from substrate functions, a signaling role of sucrose in root growth regulation is well established. This raised the question whether sucrose signals might also be involved in formation of cluster-roots (CRs) under phosphate (Pi) limitation, mediating exudation of phosphorus (P)-mobilizing root exudates, e.g. in Lupinus albus and members of the Proteaceae. Earlier studies demonstrated that CR formation in L. albus was mimicked to some extent by external application of high sucrose concentrations (25 mM) in the presence of extremely high P supply (1-10 mM), usually suppressing CR formation. In this study, we re-addressed this question using an axenic hydroponic culture system with normal P supply (0.1 mM) and a range of sucrose applications (0.25-25 mM). The 2.5mM sucrose concentration was comparable with internal sucrose levels in the zone of CR initiation in first-order laterals of P-deficient plants (3.4 mM) and induced the same CR morphology. Similar to earlier studies, high sucrose concentrations (25 mM) resulted in root thickening and inhibition of root elongation, associated with a 10-fold increase of the internal sucrose level. The sucrose analog palatinose and a combination of glucose/fructose failed to stimulate CR formation under P-sufficient conditions, demonstrating a signal function of sucrose and excluding osmotic or carbon source effects. In contrast to earlier findings, sucrose was able to induce CR formation but had no effect on CR functioning with respect to citrate exudation, in vitro activity and expression of genes encoding phosphoenolpyruvate carboxylase, secretory acid phosphatase and MATE transporters, mediating P-mobilizing functions of CRs.
引用
收藏
页码:407 / 419
页数:13
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