Abstract

The postharvest processing factors including cherry processing methods highly influence the final quality of coffee beverages, especially in the composition of several coffee metabolites such as glucose, fructose, the amino acid (glutamic acid), and chlorogenic acids (CGA) as well as trigonelline contents. In this research, UV spectroscopy combined with chemometrics was used to classify a ground roasted Lampung robusta specialty coffee according to differences in the cherry processing methods. A total of 360 samples of Lampung robusta specialty coffee with 1 g of weight for each sample from three different cherry processing methods were prepared as samples: 100 samples of pure dry coffee (DRY), 100 samples of pure semi-dry coffee (SMD), 100 samples of pure wet coffee (WET) and 60 samples of adulterated coffee (ADT) (SMD coffee was adulterated with DRY and WET coffee). All samples were extracted using a standard protocol as explained by previous works. A low-cost benchtop UV-visible spectrometer (Genesys™ 10S UV-Vis, Thermo Scientific, Waltham, MA, USA) was utilized to obtain UV spectral data in the interval of 190–400 nm using the fast scanning mode. Using the first three principal components (PCs) with a total of 93% of explained variance, there was a clear separation between samples. The samples were clustered into four possible groups according to differences in cherry processing methods: dry, semi-dry, wet, and adulterated. Four supervised classification methods, partial least squares–discriminant analysis (PLS-DA), principal component analysis–linear discriminant analysis (PCA-LDA), linear discriminant analysis (LDA) and support vector machine classification (SVMC) were selected to classify the Lampung robusta specialty coffee according to differences in the cherry processing methods. PCA-LDA is the best classification method with 91.7% classification accuracy in prediction. PLS-DA, LDA and SVMC give an accuracy of 56.7%, 80.0% and 85.0%, respectively. The present research suggested that UV spectroscopy combining with chemometrics will be highly useful in Lampung robusta specialty coffee authentication.

Highlights

  • Coffee (Coffea sp.) is a widely consumed beverage with two popular varieties being planted worldwide: arabica (Coffea arabica) with 57% of global coffee production and robusta coffee (Coffea canephora) with 43% of global coffee production [1]

  • A total of 360 samples of Lampung robusta coffee with 1 g of weight for each sample from three different cherry processing methods were prepared as samples: 100 samples of pure dry coffee (DRY), 100 samples of pure semi-dry coffee (SMD), 100 samples of pure wet coffee (WET) and 60 samples of adulterated coffee (ADT) (SMD coffee was adulterated with DRY and WET coffee)

  • It has been demonstrated that the spectral data of dry, wet, semi-dry and adulterated coffee were overlapped

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Summary

Introduction

Coffee (Coffea sp.) is a widely consumed beverage with two popular varieties being planted worldwide: arabica (Coffea arabica) with 57% of global coffee production and robusta coffee (Coffea canephora) with 43% of global coffee production [1]. In Lampung, three different robusta coffee cherry processing methods are used: dry or natural (DRY), semi-dry (SMD), and wet or washed processing (WET). Bean processing including cherry sortation (removing defective and immature fruit), cherry drying (usually using open sun drying for 3–9 days), hulling or peeling, green bean sortation (removing a defective green bean), and packing. Bean processing includes cherry sortation, pulping, fermentation (12–48 h equipped with a controlled water flow), washing, drying, peeling and polishing, green bean sortation, and packing [3,4,5]. In semi-dry processing, bean processing includes cherry sortation, pulping (without removing the mucilage), drying, peeling and polishing, green bean sortation, and packing [6]

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