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Domestic Cooking Methods Affect The Nutritional Quality of Red Cabbage
Domestic Cooking Methods Affect The Nutritional Quality of Red Cabbage
Food Chemistry
journal homepage: www.elsevier.com/locate/foodchem
a r t i c l e i n f o a b s t r a c t
Article history: The aim of this work is to investigate the effects of domestic cooking methods, including steaming, micro-
Received 6 February 2014 wave heating, boiling and stir-frying on the nutritional quality of red cabbage. Compared with fresh-cut
Received in revised form 1 April 2014 red cabbage, all cooking methods were found to cause significant reduction in anthocyanin and total
Accepted 4 April 2014
glucosinolates contents. Moreover, steaming resulted in significantly greater retention of vitamin C
Available online 13 April 2014
and DPPH radical-scavenging activity, while stir-frying and boiling, two popular Chinese cooking meth-
ods, led to significant losses of total phenolic, vitamin C, DPPH radical-scavenging activity, and total sol-
Keywords:
uble sugar as well as reducing sugars. Normally, red cabbage consumed fresh in salads could maintain the
Red cabbage
Cooking methods
highest nutrition. However, considering the habits of Asian cuisine, it is recommended to use less water
Nutrition and less cooking time, such as steaming based on our present results, so as to retain the optimum benefits
Quality of the health-promoting compounds.
Ó 2014 Elsevier Ltd. All rights reserved.
http://dx.doi.org/10.1016/j.foodchem.2014.04.025
0308-8146/Ó 2014 Elsevier Ltd. All rights reserved.
F. Xu et al. / Food Chemistry 161 (2014) 162–167 163
study is to investigate the effects of various cooking procedures on (800 ll) was added. The reaction mixture was incubated for 1 h
the nutrients and phytochemical compounds in red cabbage. at 30 °C. The absorbance was measured at 765 nm with a spectro-
photometer. Gallic acid was used as a standard.
2. Materials and methods
2.6. DPPH radical-scavenging activity assay
2.1. Plant materials
The DPPH radical-scavenging activity was carried out according
Red cabbages (B. oleracea L. var. capitata. Zaohong) were pur- to Larrauri, Sánchez-Moreno, and Saura-Calixto (1998). One gram
chased from local supermarkets (Ningbo, China). About 10 heads of frozen sample was extracted with 50% ethanol and centrifuged
of red cabbages were used in this experiment. The red cabbages at 12,000g for 10 min at 4 °C. An ethanolic solution of DPPH served
were cleaned and removed with the outer leaves of the heads, then as control. Antioxidant activity was expressed as percentage inhi-
chopped into homogeneous pieces (3 cm 3 cm) and randomly bition of the DPPH radical and was determined by the following
selected for each treatment. Each treatment was replicated three equation:
times. Abscontrol Abssample
AA ð%Þ ¼ 100:
Abscontrol
2.2. Cooking treatments
Five different cooking methods were tested: fresh-cut, boiling, 2.7. Vitamin C
steaming, microwaving and conventional stir-frying. For boiling,
300 g of homogeneous pieces of red cabbage were immersed in Vitamin C content was determined according to Kampfenkel,
800 ml of boiling water. The materials were drained off after being Vanmontagu, and Inze (1995) . One gram of frozen samples were
boiled for 5 min. For stir-frying, the blend oil (10 ml) was pre- grinded and extracted with 5 ml 5% trichloroacetic acid (TCA), then
heated to 130 °C in a wok and materials (300 g) was stir-fried for centrifuged at 10,000g for 10 min at 4 °C. A sample of the crude
5 min. For microwave, 300 g of samples were placed in a plate extract (1 ml) was added to 1 ml 5% (v/v) TCA, 1 ml 100% (v/v)
and 10 ml of water was added to prevent red cabbage from being ethanol, 0.5 ml 0.4% H3PO4, 1 ml 0.5% (v/v) 1,10-phenanthroline
burned during cooking. A microwave oven at full power (450 W) hydrate, 0.5 ml 0.03% (v/v) FeCl3, then the mixture incubated at
for 5 min was used for microwaving. Steaming was conducted by 30 °C for 1 h. The absorbance was read at 534 nm.
suspending 300 g of red cabbage above 200 ml of boiling water
for 5 min in a steamer with a lid. In addition, 300 g of red cabbage 2.8. Contents of total soluble sugar and reducing sugar
was collected for fresh-cut samples.
At the end of each cooking treatment, the materials were frozen Total soluble sugar was measured by Roe (1955) with slight mod-
by liquid nitrogen and kept in polyethylene bags at –20 °C for fur- ifications. One gram of frozen samples were grinded and extracted
ther analysis. with 5 ml of distilled water and incubated at 85 °C for 30 min, then
centrifuged at 10,000g at 4 °C. The soluble sugar content was deter-
2.3. Colour measurement mined using anthrone reagent and glucose as standard. Reducing
sugars content was determined spectrophotometrically at 540 nm
The colour of all samples was evaluated with a Minolta Chrom- with 3,5-dinitrosalicylic acid.
ameter (CR 400, Japan). The CIELAB parameters (L*, a* and b*) were
determined. L* was lightness (0–100:0 = black, 100 = white). Values 2.9. Total glucosinolates content
of a* and b* ranged from –60 to 60, where a* was negative for green
colour and positive for red colour, and b* was negative for blue and Total glucosinolates content was determined according to
positive for yellow (McGuire, 1992). Heaney, Spinks, and Fenwick (1988). The method was based on
the measurement of enzymically released glucose, which was
2.4. Total anthocyanin content hydrolysed by the enzyme myrosinase (thioglcose glycohydrolase,
EC 3.2.3.1). The content of glucose was determined by the method
Total anthocyanin content was measured by pH-differential of phenol–sulfuric acid, to assay the absorbance at 490 nm, and
spectrophotometry method following the procedure of Rapisarda, then the amount of glucosinolate can be calculated from the glu-
Fanella, and Maccarone (2000) with a slight modification. Five cose content.
grams of frozen sample was extracted with 25 ml of pH 1.0 buffer
containing 50 mM KCl and 150 mM HCl, as well as 25 ml of pH 4.5 2.10. Statistical analysis
buffer containing 50 mM sodium acetate and 240 mM HCl. Absor-
bance was measured at 510 nm and 700 nm with a spectropho- Statistical analysis was performed using the SPSS package pro-
tometer, using A = [(A510 A700) pH 1.0 (A510 A700) pH 4.5] gramme version 16.0 (SPSS Inc., Chicago, IL). All data were
with a molar extinction coefficient of cyaniding 3-glucoside of expressed as the mean ± standard error (SE) and analysis by one-
29600. Results were expressed as milligrams of Cy-3-Glu equiva- way analysis of variance (ANOVA). Differences were considered
lents per gram of fresh weight. significant at p < 0.05.
Total phenolic content was determined by the Folin–Ciocalteu 3.1. Effect of cooking methods on visual changes and surface colour in
method. One gram of frozen red cabbage sample was extracted red cabbage
with 80% acetone containing 0.2% formic acid, and the mixture
was centrifuged at 12,000g for 10 min at 4 °C. In brief, an aliquot Changes of external colour of red cabbage were evaluated
(20 ll) of sample solution was mixed with 180 ll of distilled water through L*, a* and b*. The change of colour indexes in samples with
and 1 ml of Folin–Ciocalteu reagent; 7.5% sodium carbonate different cooking methods is shown in Table 1. Compared with
164 F. Xu et al. / Food Chemistry 161 (2014) 162–167
Table 1
Colour indexes in red cabbage cooked by different methods.
All values are the means ± SE. Values not sharing a common letter are significantly different at p < 0.05.
Fig. 1. The anthocyanin content in red cabbage cooked by different methods (fresh- Fig. 3. The vitamin C content in red cabbage cooked by different methods (fresh-
cut, stir-frying, boiling, microwave, steaming). Values are the means ± SE. Vertical cut, stir-frying, boiling, microwave, steaming).Values are the means ± SE. Vertical
bars represent the standard errors of the means. Values not sharing a common bars represent the standard errors of the means. Values not sharing a common
letter are significantly different at p < 0.05. letter are significantly different at p < 0.05.
F. Xu et al. / Food Chemistry 161 (2014) 162–167 165
Fig. 5. The total glucosinolates content in red cabbage cooked by different methods
(fresh-cut, stir-frying, boiling, microwave, steaming).Values are the means ± SE.
Vertical bars represent the standard errors of the means. Values not sharing a
common letter are significantly different at p < 0.05.
fresh-cut, microwaved or steamed. In broccoli, there was a 29% loss better for human consumption habits to cook the red cabbage by
of vitamin C level when boiled, while no change was observed lightly steaming.
when steamed (Gliszczynska-Swiglo et al., 2006). Boiling and
stir-frying/boiling also caused a dramatic loss of vitamin C in broc-
Acknowledgements
coli, which was related to high temperatures, long cooking time,
enzymatic oxidation during the preparation and cooking process
This study was supported by the National Science Foundation of
and frequent stirring that expose the materials to atmospheric oxi-
China (31301574), Natural Science Foundation of Ningbo City
dation (Yadav & Sehgal, 1995). Besides, vitamin C is water soluble,
(2013A610159), National Science and Technology Support
stir-frying and boiling might cause great losses of vitamin C by
Programme (2014BAD04B00) and the Induction of Talent Project
leaching into surrounding water as well. Therefore, using minimal
(ZX2012000031) and the K.C. Wong Magna Fund at Ningbo
cooking water and cooking for shorter time periods resulted in bet-
University.
ter vitamin C retention (Erdman Jr & Klein, 1982).
Few data were available on the influence of cooking treatments
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