Related Experiment Video
Updated: Sep 19, 2025

Biosynthesis of a Flavonol from a Flavanone by Establishing a One-pot Bienzymatic Cascade
Published on: August 14, 2019
Seedy Banana - A Source of Stilbenes and Flavan-3-ols
Hoai Thi Tran1,2, Markus Bacher1, Stefano Barbini3
1Institute of Chemistry of Renewable Resources, BOKU University, Konrad-Lorenz-Straße 24, Tulln 3430, Austria.
Abstract:
This study aimed at identifying the bioactive compounds in the seeds of three seedy banana varietiesMusa acuminata, Musa itinerans, and Ensete glaucum. GC-MS of extracts and NMR of isolated compounds were used for the identification of the components and GC-MS/FID was employed for quantification. The proportion of seeds in all samples was around 50% of the dried fruit weight. The seeds were rich in piceatannol, (+)-epiafzelechin, and epiafzelechin dimers. Piceatannol and epiafzelechin dimers were reported in seedy bananas for the first time. The highest piceatannol content was found in Ensete, accounting for 713 ± 71.9 mg/100 g dry weight (DW), followed by the seeds of ripe Musa acuminata and Musa itinerans at 440 ± 56.7 and 242 ± 17.4 mg/100 g DW, respectively. Musa seeds with a higher content of piceatannol had lower concentrations of epiafzelechin and its dimers, in the ranges of 287 to 553 mg/100 g of DW and 533 to 976 mg/100 g of DW, respectively. The content depended on maturity. Compared with ripe fruits, green Musas contained hardly any piceatannol and higher levels of epiafzelechin dimers. Gallocatechin was detected only in Ensete glaucum at 145 ± 19.7 mg/100 g of DW, and a major part of the phenolic compounds in g was found in the seed coat. The identified phenolic compounds in the seeds suggest that seedy bananas could be a potential new crop for food supplements.
More Related Videos
Related Concept Videos
Fruit Development, Structure, and Function
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Seed Structure and Early Development of the Sporophyte
Source And Potency Of Stem Cells
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Drugs that Stabilize Microtubules

