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PMID: 28984366 Published · ppublish English Journal Article Review

Metabolism within the specialized guard cells of plants.

The New phytologist ·Vol. 216 ·No. 4 ·2017-12-00 ·Pages 1018-1033

Daloso DM, Medeiros DB, Dos Anjos L, Yoshida T, Araújo WL, Fernie AR

Abstract

Contents 1018 I. 1018 II. 1019 III. 1022 IV. 1025 V. 1026 VI. 1029 1030 References 1030 SUMMARY: Stomata are leaf epidermal structures consisting of two guard cells surrounding a pore. Changes in the aperture of this pore regulate plant water-use efficiency, defined as gain of C by photosynthesis per leaf water transpired. Stomatal aperture is actively regulated by reversible changes in guard cell osmolyte content. Despite the fact that guard cells can photosynthesize on their own, the accumulation of mesophyll-derived metabolites can seemingly act as signals which contribute to the regulation of stomatal movement. It has been shown that malate can act as a signalling molecule and a counter-ion of potassium, a well-established osmolyte that accumulates in the vacuole of guard cells during stomatal opening. By contrast, their efflux from guard cells is an important mechanism during stomatal closure. It has been hypothesized that the breakdown of starch, sucrose and lipids is an important mechanism during stomatal opening, which may be related to ATP production through glycolysis and mitochondrial metabolism, and/or accumulation of osmolytes such as sugars and malate. However, experimental evidence supporting this theory is lacking. Here we highlight the particularities of guard cell metabolism and discuss this in the context of the guard cells themselves and their interaction with the mesophyll cells.

Keywords
guard cells malate photosynthesis starch stomata stomatal movements sucrose water-use efficiency (WUE)
MeSH Terms
Carbohydrate Metabolism Mesophyll Cells/metabolism Photosynthesis Plant Stomata/physiology Starch/metabolism
Chemicals
Starch
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Daloso Danilo M
Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Ceará, Fortaleza, Ceará, 60451-970, Brasil.
Medeiros David B
Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am Mühlenberg 1, Potsdam-Golm, 14476, Germany. | Max-Planck Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, Viçosa, Minas Gerais, 36570-900, Brasil.
Dos Anjos Letícia
Departamento de Bioquímica e Biologia Molecular, Universidade Federal do Ceará, Fortaleza, Ceará, 60451-970, Brasil.
Yoshida Takuya
Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am Mühlenberg 1, Potsdam-Golm, 14476, Germany.
Araújo Wagner L
Max-Planck Partner Group at the Departamento de Biologia Vegetal, Universidade Federal de Viçosa, Viçosa, Minas Gerais, 36570-900, Brasil.
Fernie Alisdair R
Max-Planck-Institut für Molekulare Pflanzenphysiologie, Am Mühlenberg 1, Potsdam-Golm, 14476, Germany.
Article Info
Journal
The New phytologist
Abbr.
New Phytol
ISSN
1469-8137
Published
2017-12-00
Epub
2017-00-06
Pages
1018-1033
Language
English
Region
England
NLM ID
9882884
Subset
IM
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