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Investigating carotenoid loss after drying and storage of

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185<br />

8. Study under controlled conditions<br />

demonstrated that peroxidase activity dramatically decreased (Kamiya <strong>and</strong> Nagamune<br />

2002) <strong>and</strong> these results have been confirmed in Chapter 7. Dioxygenases known for their<br />

ability to degrade <strong>carotenoid</strong>s into aroma compounds (Auldridge et al. 2006) also lose<br />

activity in non-aqueous environments (Sanakis et al. 2003). For these different reasons,<br />

in this study, the possibility <strong>of</strong> <strong>carotenoid</strong> degradation due to enzymatic activity seemed<br />

unlikely.<br />

Oxygen<br />

Degradation <strong>of</strong> !-carotene was highly related to the oxygen level flushed through the<br />

sample as seen in Figure 8-10B. Under different levels <strong>of</strong> oxygen <strong>and</strong> at 40ºC,<br />

<strong>carotenoid</strong> degradation fitted first order kinetics (Table 8-8).<br />

Table 8-8: First order rate <strong>of</strong> <strong>carotenoid</strong> degradation <strong>of</strong> (k) expressed in day -1 at<br />

various water activities at 40ºC in dried sweet potato chips on a dry weight basis.<br />

Mean <strong>of</strong> triplicate thermal treatment (st<strong>and</strong>ard deviation). Oxygen level 21% (air).<br />

Flushed gaz N2<br />

2.5% O2:<br />

97.5% N2<br />

10% O2:<br />

90% N2<br />

21% O2:<br />

79% N2<br />

Oxygen concentration (%) 0 2.5 10 21<br />

Trans-!-carotene*<br />

k<br />

R<br />

0.0143 (0.0022) 0.0338 (0.0056) 0.0543 (0.0021) 0.0887 (0.0038)<br />

2 0.754 (0.216) 0.949 (0.020) 0.963 (0.007) 0.961 (0.012)<br />

Degradation rate constants significantly differed between samples (One way-ANOVA<br />

p

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