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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
초록

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
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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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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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1,4-Diazabicyclo[2.2.2]octane, ReagentPlus®, ≥99%
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Dabco® 33-LV
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Chloroform, ACS reagent, ≥99.8%, contains amylenes as stabilizer
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Chlorotrimethylsilane, purified by redistillation, ≥99%
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Ethanol solution, certified reference material, 2000 μg/mL in methanol
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Chloroform, suitable for HPLC, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer
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Triacontane, 98%
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Chloroform, anhydrous, contains amylenes as stabilizer, ≥99%
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Chloroform, anhydrous, ≥99%, contains 0.5-1.0% ethanol as stabilizer
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Chloroform, ReagentPlus®, ≥99.8%, contains 0.5-1.0% ethanol as stabilizer
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Hydrogen peroxide solution, contains inhibitor, 30 wt. % in H2O, ACS reagent
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Chloroform, contains ethanol as stabilizer, ACS reagent, ≥99.8%
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Hydrogen peroxide solution, contains ~200 ppm acetanilide as stabilizer, 3 wt. % in H2O
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Hydrogen peroxide solution, 50 wt. % in H2O, stabilized
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Hydrogen peroxide solution, contains inhibitor, 30 wt. % in H2O, meets USP testing specifications
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