1968
DOI: 10.1021/bi00842a042
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Optical properties of astaxanthin solutions and aggregates

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Cited by 140 publications
(134 citation statements)
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“…The colour was initially extracted under native conditions and had a peak absorbance in the blue spectrum at 634nm, which was very similar to the characteristics of the protein previously identified in this species (Nur-E-Borhan et al, 1995) and also to the properties of acrustacyanin isolated from lobster shells (Wald et al, 1948;Buchwald and Jencks, 1968). This native extract was denatured using detergents, which triggered a distinctive colour shift from 634 to 484nm, also typical of disrupting the CRCN-carotenoid interaction.…”
Section: Protein Analysis and Quantificationmentioning
confidence: 54%
“…The colour was initially extracted under native conditions and had a peak absorbance in the blue spectrum at 634nm, which was very similar to the characteristics of the protein previously identified in this species (Nur-E-Borhan et al, 1995) and also to the properties of acrustacyanin isolated from lobster shells (Wald et al, 1948;Buchwald and Jencks, 1968). This native extract was denatured using detergents, which triggered a distinctive colour shift from 634 to 484nm, also typical of disrupting the CRCN-carotenoid interaction.…”
Section: Protein Analysis and Quantificationmentioning
confidence: 54%
“…The carotenoid concentration was obtained using the Lambert-Beer law, and for calculation purposes, the following equation was applied to the absorbance values: Total carotenoid μg/mgh=(absorbance / € x molecular mass × 1,000 × sample volume L)/ sample dry weight )mg(. The specific optical extinction coefficient € 1 1cm of 124,000 (astaxanthin) at 460nm was used (Buchwaldt & Jencks, 1968) in conjunction with a molecular mass of 596.84 (astaxanthin). The absorbance measurements were performed in triplicate, and the values previously averaged were applied in the above equation (Schoefs, 2002).…”
Section: Methodsmentioning
confidence: 99%
“…Astaxanthin actually forms three stereoisomers, based on the angle of the hydroxyl groups to the rings, but all are similarly dichroic to linearly polarized light (two of these stereoisomers also show circular dichroism, which is not relevant here). In biological membranes, molecules of astaxanthin are of the correct size to span the lipid bilayer, and thus sit vertically within the membrane with the hydrophilic ring structures embedded in the glycerol surfaces of biomembranes and the hydrophobic conjugated axis extending through the internal phospholipid tails 13,14 . Thus, in flat membrane layers, all the dipole axes of the astaxanthin molecules are parallel but are perpendicular to the plane of the membrane.…”
Section: Polarizers Based On the Dichroic Carotenoid Molecule Astaxamentioning
confidence: 99%