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  • Confocal laser scanning microscopy elucidation of the micromorphology of the leaf cuticle and analysis of its chemical composition.

Confocal laser scanning microscopy elucidation of the micromorphology of the leaf cuticle and analysis of its chemical composition.

Protoplasma (2015-02-26)
Pavani P Nadiminti, James E Rookes, Ben J Boyd, David M Cahill
ABSTRACT

Electron microscopy techniques such as transmission electron microscopy (TEM) and scanning electron microscopy (SEM) have been invaluable tools for the study of the micromorphology of plant cuticles. However, for electron microscopy, the preparation techniques required may invariably introduce artefacts in cuticle preservation. Further, there are a limited number of methods available for quantifying the image data obtained through electron microscopy. Therefore, in this study, optical microscopy techniques were coupled with staining procedures and, along with SEM were used to qualitatively and quantitatively assess the ultrastructure of plant leaf cuticles. Leaf cryosections of Triticum aestivum (wheat), Zea mays (maize), and Lupinus angustifolius (lupin) were stained with either fat-soluble azo stain Sudan IV or fluorescent, diarylmethane Auramine O and were observed under confocal laser scanning microscope (CLSM). For all the plant species tested, the cuticle on the leaf surfaces could be clearly resolved in many cases into cuticular proper (CP), external cuticular layer (ECL), and internal cuticular layer (ICL). Novel image data analysis procedures for quantifying the epicuticular wax micromorphology were developed, and epicuticular waxes of L. angustifolius were described here for the first time. Together, application of a multifaceted approach involving the use of a range of techniques to study the plant cuticle has led to a better understanding of cuticular structure and provides new insights into leaf surface architecture.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Auramine O, Dye content ≥80 %, certified by the Biological Stain Commission
Sigma-Aldrich
Pyridine, anhydrous, 99.8%
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Pyridine, ≥99%
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Auramine O, Dye content 85 %, certified by the Biological Stain Commission
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Chlorotrimethylsilane solution, 1.0 M in THF
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Nitrogen, ≥99.998%
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Orotidine 5′-monophosphate trisodium salt, ≥99% (HPLC), powder
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Pyridine, ACS reagent, ≥99.0%
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Pyridine, ACS reagent, ≥99.0%
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Pyridine, biotech. grade, ≥99.9%
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Pyridine, ReagentPlus®, ≥99%
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Pyridine, puriss. p.a., ACS reagent, reag. Ph. Eur., ≥99.5% (GC)
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Pyridine, ReagentPlus®, ≥99%
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Ethanol, puriss. p.a., absolute, ≥99.8% (GC)
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Ethyl alcohol, Pure, 200 proof, ACS reagent, ≥99.5%
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Chloroform, ≥99%, PCR Reagent, contains amylenes as stabilizer
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Hydrogen peroxide solution, 30 % (w/w) in H2O, contains stabilizer
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1,4-Diazabicyclo[2.2.2]octane, ReagentPlus®, ≥99%
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Dabco® 33-LV
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Chlorotrimethylsilane, ≥98.0% (GC)
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Chlorotrimethylsilane, produced by Wacker Chemie AG, Burghausen, Germany, ≥99.0% (GC)
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Hydrogen peroxide solution, 34.5-36.5%
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Chloroform, puriss. p.a., ACS reagent, ≥99.8% (chloroform + ethanol, GC)
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Chlorotrimethylsilane, purified by redistillation, ≥99%
Supelco
Chloroform, suitable for HPLC, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer
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Chloroform, ACS reagent, ≥99.8%, contains amylenes as stabilizer
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Triacontane, 98%
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Chloroform, anhydrous, ≥99%, contains 0.5-1.0% ethanol as stabilizer
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Chloroform, anhydrous, contains amylenes as stabilizer, ≥99%
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Hydrogen peroxide solution, contains potassium stannate as inhibitor, 30-32 wt. % in water, semiconductor grade, 99.999% trace metals basis