A response surface method was used to optimize the microwave-assisted extraction parameters such as extraction time (t) (min), solvent (methanol) concentration (S) (v/v) and microwave power level (MP) for extraction of antioxidants from potato peels. Max. total phenolics content of 3.94 mg g−1 dry weight (dw) was obtained at S of 67.33%, t of 15 min and a MP of 14.67%. For ascorbic acid (1.44 mg g−1 dw), caffeic acid (1.33 mg g−1 dw), ferulic acid (0.50 mg g−1 dw) max contents were obtained at S of 100%, t of 15 min, and MP of 10%, while the max chlorogenic acid content (1.35 mg g−1 dw) was obtained at S of 100%, t of 5 min, and MP of 10%. The radical scavenging activity of the extract was evaluated by using the DPPH assay and optimum antioxidant activity was obtained at S of 100%, t of 5 min, and MP of 10%.
The enzymatic transesterification of selected phenolic acids with TAG, including trilinolein (TLA) and trilinolenin (TLNA), was investigated in an organic solvent medium. Maximal bioconversion of 66% was obtained with a dihydrocaffeic acid (DHCA) to TLA ratio of 1:2 after 5 d of reaction. Similarly, the highest bioconversion of 62% was obtained with a DHCA to TLNA ratio of 1:2, but after 12 d of reaction. However, a ratio of 1:4 DHCA/TLA decreased the bioconversion to 53%. Transesterification reactions of ferulic acid with both TAG, using a ratio of 1:2, resulted in low bioconversion of 16 and 14% with TLA and TLNA, respectively. The overall results indicated that bioconversion of phenolic MAG was higher than that of phenolic DAG. The structures of mono-and dilinoleyl dihydrocaffeate as well as those of mono-and dilinolenyl dihydrocaffeate were confirmed by LC-MS analyses. The phenolic lipids demonstrated moderate radical-scavenging activity. FIG. 2. HPLC chromatograms of the samples of the enzymatic transesterification reactions of DHCA with TLA (A and B) and trilinolenin (TLNA) (A′ and B′) monitored at 280 and 215 nm. Peak numbers were identified as follows: dihydrocaffeic acid, #1 and 1′; TLA, #7; TLNA, #7'; phenolic MAG, #2 and 2'; phenolic DAG, #5 and 5'; MAG, #3 and 3'; DAG, #6 and 6'; side reaction product, #4; and TLNA oxidation product, #8′. LIPASE-CATALYZED TRANSESTERIFICATION OF TRILINOLEIN AND TRILINOLENIN 105 JAOCS, Vol. 83, no. 2 (2006) FIG. 3. Atmospheric pressure chemical ionization MS analysis of monolinoleyl dihydrocaffeate (A), dilinoleyl dihydrocaffeate (B), monolinolenyl dihydrocaffeate (A'), and dilinolenyl dihydrocaffeate (B′). FIG. 4. Progress curves of the biosynthesis of phenolic MAG (I), phenolic DAG (I I), and total phenolic lipids (L) as well as the hydrolysis of TAG (L L) during the lipase-catalyzed transesterification of dihydrocaffeic acid with TLA (A) and TLNA (B).
A dynamic human gastrointestinal (GI) model was used to digest cooked tubers from purple-fleshed Amachi and Leona potato cultivars to study anthocyanin biotransformation in the stomach, small intestine and colonic vessels. Colonic Caco-2 cancer cells and non-tumorigenic colonic CCD-112CoN cells were tested for cytotoxicity and cell viability after 24 h exposure to colonic fecal water (FW) digests (0%, 10%, 25%, 75% and 100% FW in culture media). After 24 h digestion, liquid chromatography-mass spectrometry identified 36 and 15 anthocyanin species throughout the GI vessels for Amachi and Leona, respectively. The total anthocyanin concentration was over thirty-fold higher in Amachi compared to Leona digests but seven-fold higher anthocyanin concentrations were noted for Leona versus Amachi in descending colon digests. Leona FW showed greater potency to induce cytotoxicity and decrease viability of Caco-2 cells than observed with FW from Amachi. Amachi FW at 100% caused cytotoxicity in non-tumorigenic cells while FW from Leona showed no effect. The present findings indicate major variations in the pattern of anthocyanin breakdown and release during digestion of purple-fleshed cultivars. The differing microbial anthocyanin metabolite profiles in colonic vessels between cultivars could play a significant role in the impact of FW toxicity on tumor and non-tumorigenic cells.
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