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Production Practices and Quality Assessment of Food Crops. Vol. 1

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16 R. M. Madakadze <strong>and</strong> J. Kwaramba<br />

Table 6. Effect <strong>of</strong> increasing potassium concentrations in potato tubers, on the composition <strong>and</strong><br />

quality <strong>of</strong> the tubers.<br />

Type <strong>of</strong> change Effect <strong>of</strong> increasing Responsible mechanism<br />

Potassium<br />

Water content Increase Osmoregulation<br />

Reducing sugars Decrease Osmoregulation<br />

Citric acid Increase Cation-anion balance<br />

Starch Decrease<br />

Black spot disorder Decrease Lower polyphenol oxidase activity<br />

Darkening <strong>of</strong> press sap Decrease High citric acid/low polyphenol oxidase<br />

Discoloration after cooking Decrease High citric acid/low chlorogenic acid<br />

Storage loss Decrease Lower respiration <strong>and</strong> fungal diseases<br />

Adapted from Marschner (1989).<br />

(Lauchli <strong>and</strong> Pfluger, 1978), starch synthase (Nitsos <strong>and</strong> Evans, 1969), <strong>and</strong><br />

membrane bound ATPases (which requires Mg 2+ but are further stimulated by K + ).<br />

Potassium is required for protein synthesis in higher plants. The role <strong>of</strong> K + in protein<br />

synthesis is reflected in the accumulation <strong>of</strong> soluble nitrogen compounds, (e.g. amino<br />

acids, amides <strong>and</strong> nitrate) in K-deficient plants (Mengel <strong>and</strong> Halal, 1968).<br />

In higher plants K + affects photosynthesis at various levels. K + is the dominant<br />

counter ion to light induced H + flux across the thylakoid membranes <strong>and</strong> the<br />

establishment <strong>of</strong> the transmembrane pH gradient necessary for the synthesis <strong>of</strong><br />

ATP (photophosphorylation) (Lauchli <strong>and</strong> Pfluger, 1978). An increase in the leaf<br />

potassium content is accompanied by increased rates <strong>of</strong> photosynthesis, photorespiration<br />

<strong>and</strong> RuBP carboxylase activity, but a decrease in dark respiration. In most<br />

plant species K + also has the major responsibility for turgor changes in the guard<br />

cells during stomatal movement. An increase in the K + concentration in the guard<br />

cells results in the uptake <strong>of</strong> water from the adjacent cells <strong>and</strong> thus stomatal opening<br />

(Humble <strong>and</strong> Raschke, 1971).<br />

3.3.3. Boron<br />

Boron occurs mainly as boric acid, H 3BO 3 a very weak acid in aqueous solution.<br />

At physiological pH (< 8) mainly the undissociated boric acid is present in the<br />

soil or nutrient solution. This is also the preferred form taken up by the roots.<br />

Boron is strongly complexed to cell wall constituents even in the roots (Thelier et<br />

al., 1979). Long distance transport <strong>of</strong> boron from the roots to the shoot is confined<br />

to the xylem, <strong>and</strong> uptake <strong>and</strong> translocation are closely related not only to the mass<br />

flow <strong>of</strong> water to the root surface but also to the xylem water flow. There is no<br />

indication that boron is an enzyme component <strong>and</strong> there is only little evidence<br />

(Birnbaum et al., 1977) that the activity <strong>of</strong> any enzyme is enhanced or inhibited<br />

by boron. Interactions between boron <strong>and</strong> other mineral nutrients during uptake<br />

<strong>and</strong> in the plant itself seem to be <strong>of</strong> minor importance (Marschner, 1989).<br />

Bo deficiency is a widespread nutritional disorder in vegetables. Boron deficiency<br />

usually occurs under:

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