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Correction to "Biosynthesis-Based Spatial Metabolome of Condensed Tannin Reveals Its Role in Salt Tolerance of Non-Salt-Secretor Mangrove Kandelia Obovata". [PDF]
Plant Cell Environeuropepmc +1 more source
Veinal–mesophyll interaction under biotic stress
Journal of Plant Physiology, 2015 According to microscopic observations, germinating hyphae of Botrytis cinerea, though easily penetrating Mesembryanthemum crystallinum mesophyll tissue, are limited in growth in mid-ribs and only occasionally reach vascular bundles. In mid-ribs of C3 and CAM leaves, we found significantly lower rbcL (large RubisCO subunit) abundance.
Nosek, Michał +5 more
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The Plant Journal, 2021
SummaryStromules are dynamic membrane‐bound tubular structures that emanate from plastids. Stromule formation is triggered in response to various stresses and during plant development, suggesting that stromules may have physiological and developmental roles in these processes. Despite the possible biological importance of stromules and their prevalence
Ryuuichi D. Itoh +6 more
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SummaryStromules are dynamic membrane‐bound tubular structures that emanate from plastids. Stromule formation is triggered in response to various stresses and during plant development, suggesting that stromules may have physiological and developmental roles in these processes. Despite the possible biological importance of stromules and their prevalence
Ryuuichi D. Itoh +6 more
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Differentiation of Mesophyll and Paraveinal Mesophyll in Soybean Leaf
Botanical Gazette, 1991The paraveinal mesophyll (PVM) in trifoliolate soybean leaves is a one-cell-thick reticulum extending between the vascular bundles at phloem level. This study describes various features of PVM differentiation in relation to other tissues during leaf ontogeny and also gives quantitative data on cell, vacuole, cytoplasm, and nucleus compartment size in ...
Karen A. Liljebjelke +1 more
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Scalable Transfection of Maize Mesophyll Protoplasts
Journal of Visualized Experiments, 2023The transfection of maize mesophyll cells often involves digesting the plant cell walls to create protoplasts and then inserting DNA via electroporation or polyethylene glycol (PEG). Previous methods were developed to produce tens of thousands of transfected protoplasts at once.
Jackson, Tonnies +4 more
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Microbodies in conifer needle mesophyll
Protoplasma, 1974Microbodies are described in the mesophyll tissue of several conifer species. Cytochemical staining ofPinus strobus andPicea mariana with 3,3′ diaminobenzidine indicated the presence of catalase in microbodies. In older tissue microbody staining was variable with peroxidative activity occurring in mesophyll cell walls and the cytoplasm.
J F, Chabot, B F, Chabot
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Evacuolation of mesophyll protoplasts
Plant Science Letters, 1983Abstract The differential sedimentation of mesophyll protoplasts through a continous Percol gradient can lead to 100% evacuolation of protoplasts which subsequently could be regenerated to whole plants.
R.J Griesbach, K.C Sink
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Plant Science Letters, 1981
Abstract Protoplasts were released from approx. 99% of mechanically isolated soybean primary leaf cells within 1 h in a mixture of 0.1% Pectolyase, 0.2% cellulase, 8% mannitol and 0.12% CaCl 2 .2H 2 O, at pH 5.8 and 30°C.
F.W Schwenk, C.A Pearson, M.R Roth
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Abstract Protoplasts were released from approx. 99% of mechanically isolated soybean primary leaf cells within 1 h in a mixture of 0.1% Pectolyase, 0.2% cellulase, 8% mannitol and 0.12% CaCl 2 .2H 2 O, at pH 5.8 and 30°C.
F.W Schwenk, C.A Pearson, M.R Roth
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Dipeptide transport in barley mesophyll vacuoles
Planta, 1995The transport of [14C]glycyl-glycine (Gly-Gly) across the tonoplast of isolated barley vacuoles has been characterized. Uptake of the dipeptide Gly-Gly into barley mesophyll vacuoles was strongly increased by the addition of ATP, while Mg2+ inhibited the ATP-dependent fluxes.
A, Jamaï +3 more
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Response to chilling of tomato mesophyll protoplasts
Planta, 1981Freshly isolated protoplasts from tomato leaves show two completely different responses to a chilling treatment of 12 h at 7° C prior to culture at 29° C, depending on the presence or absence of glucose in the medium. In the culture medium with glucose as osmoticum, where the rate of cell divisions under optimal culture conditions is relatively high ...
H P, Mühlbach, H, Thiele
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