Spelling suggestions: "subject:"carotenes"" "subject:"carotene's""
1 |
Oxidative degradation of Beta-caroteneChiba, Naoki 07 October 1966 (has links)
The role of beta-carotene degradations in the development of
off-flavors in milk and milk products has not been established. The
purpose of this investigation was to study the oxidation of beta-carotene
and to identify volatile compounds arising from autoxidizing
beta-carotene.
Pure cyrstalline beta-carotene, mixed with Celite to accelerate
oxidation, was oxidized at 50°C by molecular oxygen in two different
systems. The peroxide value and loss of beta-carotene were measured
after controlled oxidation periods. In one system the maximum
peroxide value, 295 milliequivalents per 1,000 grams, occurred
after three hours of oxidation. In the other system the maximum
peroxide value, 586 milliequivalents per 1,000 grams, was observed
after six hours of oxidation. Approximately 80 percent of the beta-carotene
was decomposed within the first ten hours of oxidation.
Volatile compounds from autoxidizing beta-carotene were
collected by a cold-trap gas-entrainment technique. The collected compounds were subjected to gas-liquid chromatography and rapidscan
mass spectrometry, and the following compounds were identified:
n-pentane, ethyl ether, acetaldehyde, acetone, propanal,
methyl vinyl ketone, toluene, isobutanal, 2-octanone and acetic
acid. Compounds tentatively identified included diacetyl, 3-methyl-
2-pentanone, 4-methyl-3-pentan-2-one, 2-methylfuran, 1,3,3-trimethylcyclohexene,
rnethyl formate, butanone, 2-methyl-2-heptenal,
1, 3-dimethyl-2-ethylcyclohexane, 2-ethyl-2-hexenal, 2-formyl-3, 3-
dimethylcyclohexene, 1, 1, 3-trimethyl-2-n-propylcyclohexane, 2-
methyl-3-nonene and 3, 5, 5-trimethyl-4-(4'-butyl-3'-en-2'-onyl)
cyclohexa-1, 3-diene. A fraction possessing a strong "nutty" aroma
was tentatively identified as 2-methyl-2-heptenal. The volatile compounds
identified can be predicted as degradation products of beta-carotene
oxidation. / Graduation date: 1967
|
2 |
Effect of kind of carrier and physical state of the carrier on the absorption and utilization of carotene by dairy calvesCrowley, J. W. January 1951 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1951. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 103-115).
|
3 |
Carotene requirements of the pigHentges, J. F. January 1952 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1952. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
|
4 |
Analysis of carotenes in dark orange carrot roots, Daucus carota, L.Wolff, Xenia Yvette. January 1984 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1984. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 127-131).
|
5 |
The stability of carotene and vitamin A in mixed poultry rations and the comparative efficiency of these components for egg production and hatchability.Parkinson, Leonard Raymond 01 January 1947 (has links) (PDF)
No description available.
|
6 |
Factors affecting carotene content of alfalfaHackerott, Harold Leroy January 2011 (has links)
Typescript, etc. / Digitized by Kansas State University Libraries
|
7 |
A study of the phasic separation of chlorophyll and caroteneGreen, Troy Ren. January 1952 (has links)
Call number: LD2668 .T4 1952 G73 / Master of Science
|
8 |
Effect of various lipids on carotene stability of dehydrated alfalfa mealAlvarez, Brunilda Cox. January 1961 (has links)
Call number: LD2668 .T4 1961 A47
|
9 |
The role of carotenogenesis in the response of the green alga haematococcus pluvialis to oxidative stressLi, Yantao., 李彥韜. January 2007 (has links)
published_or_final_version / abstract / Biological Sciences / Doctoral / Doctor of Philosophy
|
10 |
Relation of color in cooked carrots to carotene content as determined by chromatographic and spectrophotometric methodsBorchgrevink, Nancy Carter 13 April 1964 (has links)
Carrots were cooked to the just tender stage in a saucepan and
in a pressure saucepan for appropriate lengths of time to make them
approximately equal in tenderness as determined by a panel of
judges and the Kramer Shear Press. A third lot of carrots was
cooked in a pressure saucepan for approximately twice as long to
represent overcooked carrots. Judges and the Hunter Color Meter
indicated that the carrots cooked in the saucepan were more typically
red-orange and bright and the carrots overcooked in the pressure
saucepan were more yellow and dull.
Pigments extracted from the carrots from the three cooking
treatments were chromatographed on a magnesia column and the
principle fractions, α-carotene and β-carotene, eluted. The β-carotene was rechromatographed on an alumina column to separate it into all-trans-β-carotene and neo-β-carotene B. In absolute amounts,
carrots cooked in the saucepan had the highest concentration
of all-trans-β-carotene and the highest total of all-trans-β-carotene,
neo-β-carotene B and α-carotene, followed by those carrots cooked in
the pressure saucepan for 50 seconds, with those cooked in the pressure
saucepan for two minutes being lowest in both all-trans-β-carotene
and total carotenes. However, when the a-carotene, the neo-pcarotene
B and the all-trans-β-carotene were considered as percentages
of the total, the percentage of α-carotene remained constant in
the three treatments. Carrots cooked in the pressure saucepan for
two minutes had a lower percentage of all-trans-β-carotene and a
higher percentage of neo-β-carotene B than did carrots from the
other two treatments. Thus, longer cooking in the pressure saucepan
caused greater conversion of the more vivid all-trans-β-carotene to
the paler cis-isomer, neo-β-carotene B. This isomerization plus
loss of total pigment accounts for the differences in color of the cooked
carrots from the three treatments. / Graduation date: 1964
|
Page generated in 0.05 seconds