The Yield, Fruit Quality and Some of Nutraceutical Characteristics of Saskatoon Berries (Amelanchier alnifolia Nutt.) in the Conditions of Eastern Poland
Abstract
:1. Introduction
2. Materials and Methods
2.1. Phenological Phases
2.2. Meteorological Conditions
2.3. Analytical Methods
- Average fruit mass (g)—measured on a TP 200 (OHAUS Europe GmbH, Nänikon, Switzerland) analytical balance.
- Fruit diameter (mm)—immediately after the harvest, the diameter of the fruit was measured in two directions with a caliper. Then, the obtained results from each fruit were averaged.
- Soluble solid content (SSC) (Brix degrees)—measured, according to the Polish PN-EN 012143: 2000 standard [22], in juice squeezed from 30 fruits per replication. The SSC was determined using an Atago PR-32 digital refractometer (Atago, Tokyo, Japan).
- Fruit firmness (FF) was determined as a value of the force necessary for penetration the fruit by 4.5 mm diameter punch probe. Determinations were made using an Instron type 5542 tester (Instron, High Wycombe, UK). FF was determined on 20 fruits in 3 replications. Each fruit was subjected one times (in the horizontal plane), with compression speed 240 mm−1 during penetration to 3 mm depth. FF was expressed in newton (N).
- Content of pro-health components: All reagents were of analytical purity gradients or of HPLC grade purchased from Sigma-Aldrich (Poznań, Poland) or Merck (Warsaw, Poland).
- Analysis of the total polyphenol content: According to the Waterhouse method [23], the total polyphenol level was measured with a Marcel s330 PRO spectrophotometer (Marcel S.A., Warsaw, Poland) using Folin–Ciocalteau reagent. 5 g of material crushed in liquid nitrogen were extracted with 50 mL of 100% methanol. The extraction process was repeated twice collecting the extracts into a 100 mL flask. Successively, 1 mL of extract was collected into a 50 mL flask, 35 mL of H2O, 2.5 mL of Folin–Ciocalteau reagent, and 7.5 mL of 10% NaCO3 were added. H2O was made up and incubated for 20 min at 25 ± 2 °C. All measurements were performed at a wavelength of 750 nm. Gallic acid was used as the standard at different concentrations: 0.00, 0.05, 0.15, 0.20, 0.25, and 0.3 g/L. The contents of total polyphenols is given in milligrams of gallic acid per 100 g of fresh weight.
- Analysis of the flavonoid content: Determined according to the modified method of Marinova et al. [24]. For the determination of flavonoids, 5 g of fruit ground in liquid nitrogen was used. The samples were mixed with 25 mL of 80% methanol and extracted for 15 min. Extractions were carried out two times. Distilled water, 5% NaNO2, 10% AlCl3, and 1M NaOH were added to the obtained samples successively at fixed time intervals. Measurement was performed using a Marcel s330 PRO spectrophotometer (Marcel S.A., Warsaw, Poland) at 510 nm. Total flavonoid content of fruits was expressed as mg catechin equivalents (CE) per 100 g of fresh weight of fruit.
- Analysis of the total anthocyanin content: Determined spectrophotometrically according to the method of Fuleki and Francis [25]. The method developed consists of extracting the anthocyanins with ethanol-1.5 N hydrochloric acid (85:15). 5 g of fruit crushed in liquid nitrogen was extracted in the extraction mixture for 12 h in the dark. Total anthocyanins were determined by performing two measurements at varying pH. In the first 25 mL flask, 5 mL of extract and 20 mL of pH 4.5 buffer were mixed. In the second flask (25 mL), 5 mL of extract, 5 mL of HCL and 15 mL of H2O (pH 1.0) were combined. Absorbance measurement was carried out on a Marcel spectrophotometer (Marcel S.A., Warsaw, Poland), and determinations were made at a wavelength of 535 nm. The results were expressed in mg of cyanidin-3-glucosid equivalent (AAE) per g of fresh weight.
- Qualitative and quantitative analysis of anthocyanins: The fruit homogenate was extracted with 25 mL of mixture (acetone;methanol;water = 35:35:30) acidified with 1 mL of HCl at 36%. The solution was then drained, and the clear filtrate was evaporated under vacuum at 40 °C until the acetone and methanol evaporated. The remaining solution was poured into a 25 mL flask, made up with distilled water, and the resulting sample was cleaned on a 0.45 µm Millex HV filter (Millipore, Warsaw, Poland). The identification and quantitative analysis of anthocyanins were conducted separately using the HPLC technique described by Szpadzik et al. [26], performed by means of a PerkinElmer series 200 HPLC with a Diode Array Detector (Perkin Elmer, Krakow, Poland), using a LiChroCART® 125-3 (Merck KGaA, Darmstadt, Germany) column with a 1.0 mL/min flow rate, detected at 520 nm. The mobile phase was a mixture: water (A): 20% formic acid (B): acetonitrile (C) with variable parameters of the gradient A and C. The anthocyanin content is given milligrams per 100 g of fresh weight of fruit as cyanidin-3-glucosid equivalent.
2.4. Statistical Analysis
3. Results
3.1. Phenological Phases and Meteorological Conditions during the Experiment
3.2. Yield
3.3. Fruit Mass
3.4. Fruit Diameter
3.5. Soluble Solid Content (SSC)
3.6. Fruit Firmness
3.7. Total Polyphenol Content
3.8. Total Flavonoid Content
3.9. Anthocyanin Content
3.10. Contents of Individual Anthocyanin Compounds
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Variety | 2017 | 2018 | ||
---|---|---|---|---|
Blooming Time | Harvest Time | Blooming Time | Harvest Time | |
Honeywood | 19–27 April | 19 June | 22–29 April | 17 June |
Pembina | 22–30 April | 14 June | 24 April–1 May | 11 June |
Martin | 21–29 April | 13 June | 24 April–3 May | 12 June |
Year | Cultivar | Cyanidin-3- galactoside | Cyanidin-3- glucoside | Cyanidin-3- arabidoside | Cyanidin-3- xyloside | ||||
---|---|---|---|---|---|---|---|---|---|
2017 | Honeywood | 122.75 | ±3.7 a * | 18.02 | ±0.8 b | 8.91 | ±2.2 b | 8.82 | ±0.9 a |
Pembina | 71.80 | ±4.8 b | 21.65 | ±1.8 ab | 12.21 | ±3.1 ab | 9.87 | ±0.7 a | |
Martin | 110.00 | ±4.1 a | 31.87 | ±3.4 a | 17.23 | ±1.6 a | 13.62 | ±4.0 a | |
Average for Cultivars | 101.51 A ^ | 23.84 B | 12.78 C | 10.77 C | |||||
2018 | Honeywood | 83.21 | ±2.1 a | 13.00 | ±4.2 b | 5.83 | ±1.9 b | 6.22 | ±1.4 b |
Pembina | 95.00 | ±3.7 a | 30.00 | ±1.2 a | 18.11 | ±2.5 a | 13.60 | ±0.5 a | |
Martin | 93.10 | ±4.4 a | 39.20 | ±1.5 a | 19.30 | ±1.6 b | 15.11 | ±0.8 a | |
Average for Cultivars | 90.43 A | 27.40 B | 14.41 C | 11.64 C |
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Szpadzik, E.; Krupa, T. The Yield, Fruit Quality and Some of Nutraceutical Characteristics of Saskatoon Berries (Amelanchier alnifolia Nutt.) in the Conditions of Eastern Poland. Agriculture 2021, 11, 824. https://doi.org/10.3390/agriculture11090824
Szpadzik E, Krupa T. The Yield, Fruit Quality and Some of Nutraceutical Characteristics of Saskatoon Berries (Amelanchier alnifolia Nutt.) in the Conditions of Eastern Poland. Agriculture. 2021; 11(9):824. https://doi.org/10.3390/agriculture11090824
Chicago/Turabian StyleSzpadzik, Ewa, and Tomasz Krupa. 2021. "The Yield, Fruit Quality and Some of Nutraceutical Characteristics of Saskatoon Berries (Amelanchier alnifolia Nutt.) in the Conditions of Eastern Poland" Agriculture 11, no. 9: 824. https://doi.org/10.3390/agriculture11090824
APA StyleSzpadzik, E., & Krupa, T. (2021). The Yield, Fruit Quality and Some of Nutraceutical Characteristics of Saskatoon Berries (Amelanchier alnifolia Nutt.) in the Conditions of Eastern Poland. Agriculture, 11(9), 824. https://doi.org/10.3390/agriculture11090824