4. Discussion
4.1. Light influence on cut-edge browning and water loss
We observed that high (150 μmol m−2 s −1 ) and medium (50 μmol m−2 s −1 ) continuous light intensity inhibited the cut-edge browning of fresh-cut lettuces during a 7 d storage period (Fig. 2). These results are in agreement with Zhan et al. who reported that continuous light around 35 μmol m−2 s −1 intensity decreased the browning of fresh-cut romaine lettuce and fresh-cut celery (Zhan et al., 2012, 2013c) In this study, we also experimented 2 d intermittent light treatments (2 h on/2 h off) followed by a 5 d storage in darkness (LD). The 150 LD treatment also inhibited the cut-edge browning although the salads are placed in the dark for 5 days. This result demonstrated that the effect of light was residual and was maintained in the dark. Interestingly, the lettuce treated by the 50 μmol m−2 s −1 intermittent light (50 LD) showed a slight cut-edge browning only at the end of storage (days 7). Thus, the inhibition of browning increased as the light intensity increased and the residual effect was also dependent of the light intensity. The effect of light intensity was described in model systems by Manzocco et al. (Manzocco et al., 2009). However the mechanism of action of light was not known precisely. Manzocco et al. said that visible light could inactivate polyphenol oxidase (PPO) activity due to nonreversible structural changes. Zhan et al. (2013b) have proposed that samples exposed to light could contain more ascorbic acid than those stored in darknessand inhibit the catalytic action of PPO by decreasing the pH value below the enzyme activity optimum. Several other hypotheses can be proposed: (1) light can act to inhibit PPO neosynthesis following cutting, (2) it can alter the pathways of synthesis of phenolic compounds and reduce the amounts of oxidizable phenols, and (3) it may also contribute to reducing browning due to a slight dehydration of the surface of the cuts.