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The lipid content was measured in duplicate for each sample.
Intracellular RNA content was measured by PCA method.
The ash content was measured in triplicate for each sample.
Pro content was measured according to Bates et al. (1973).
Amylose content was measured as described by Niu (1990).
Flavonoids content was measured referring to Yao et al. [23].
Chlorophyll content was measured using the duckweed fronds.
The supernatant Hb content was measured.
DNA content was measured using Cytomation Summit software (Dako).
Protein content was measured according to the Lowry method.
Iron content was measured as previously described [20].
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