A method for analysing small samples of floral pollen for free and protein‐bound amino acids

• Published in: Methods in ecology and evolution Vol. 9; no. 2; pp. 430 - 438
• Main Authors: Stabler, Daniel, Power, Eileen F., Borland, Anne M., Barnes, Jeremy D., Wright, Geraldine A., Carvalheiro, Luísa
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01-02-2018; John Wiley and Sons Inc
• Subjects: acid hydrolysis; Amino acid composition; Amino acids; Bees; Biochemistry in Ecology; Bumblebees; Essential nutrients; High performance liquid chromatography; Lipids; Liquid chromatography; microwave hydrolysis; Minerals; Nutrient content; Nutrients; Nutrition; Pollen; pollen amino acids; pollen nutrition; pollen wash; Pollinators; protein hydrolysis; Proteins; UHPLC; Vitamins; microwave hydrolysis; pollen amino acids; protein hydrolysis; UHPLC; acid hydrolysis; pollen nutrition; pollen wash
• ISSN: 2041-210X; 2041-210X
• DOI: 10.1111/2041-210X.12867

Pollen provides floral visitors with essential nutrients including proteins, lipids, vitamins and minerals. As an important nutrient resource for pollinators, including honeybees and bumblebees, pollen quality is of growing interest in assessing available nutrition to foraging bees. To date, quantifying the protein‐bound amino acids in pollen has been difficult and methods rely on large amounts of pollen, typically more than 1 g. More usual is to estimate a crude protein value based on the nitrogen content of pollen, however, such methods provide no information on the distribution of essential and non‐essential amino acids constituting the proteins.
Here, we describe a method of microwave‐assisted acid hydrolysis using low amounts of pollen that allows exploration of amino acid composition, quantified using ultra high performance liquid chromatography (UHPLC), and a back calculation to estimate the crude protein content of pollen.
Reliable analysis of protein‐bound and free amino acids as well as an estimation of crude protein concentration was obtained from pollen samples as low as 1 mg. Greater variation in both protein‐bound and free amino acids was found in pollen sample sizes <1 mg. Due to the variability in recovery of amino acids in smaller sample sizes, we suggest a correction factor to apply to specific sample sizes of pollen in order to estimate total crude protein content.
The method described in this paper will allow researchers to explore the composition of amino acids in pollen and will aid research assessing the available nutrition to pollinating animals. This method will be particularly useful in assaying the pollen of wild plants, from which it is difficult to obtain large sample weights.