A Simple and Effective Method for Observing Starch in Whole Plant Cells and in Raw and Processed Food Ingredients

Abstract

Abstract A method is described which uses cyclohexanediaminetetraacetic acid (CDTA) to produce numerous separated whole cells from plant tissue. CDTA chelates divalent cations that cross‐link the pectic polysaccharides of the middle lamella, allowing gentle separation of the cells without harsh physical treatments. These individual cells are ideal for observing starch granules in situ by microscopy without the requirement for fixation, embedding, sectioning, or prior starch extraction. Starch can easily be observed either unstained, or by polarizing optics, or after staining with iodide (I 2 /KI). Staining with I 2 /KI in combination with polarizing optics gives information on polarizing colors that indicate compositional differences within granules. Examples of the starch complement in developing, mature, and cooked rr wrinkled pea cells, and in banana and potato tissue are shown. The CDTA‐separation method is ideal for the survey of starch mutants and other cell components as it preserves cytoplasmic organization and prevents microbial degradation during storage.

Plant phenotyping relevance

植物組織から細胞を分離し、顕微鏡でデンプン顆粒を観察する方法自体が中心であり、デンプン変異体の調査など植物形質評価への再利用性が示されている。

Code and data availability

This microscopy-based starch observation paper deposits no public datasets, images, code, or models. Its Data Availability Statement says data are available only from the corresponding author upon reasonable request, so any paper-specific assets would require contacting the authors.

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