scholarly journals Informatic prediction of Cheddar cheese flavor pathway changes due to sodium substitution

2013 ◽  
Vol 350 (2) ◽  
pp. 231-238 ◽  
Author(s):  
Balasubramanian Ganesan ◽  
Kelly Brown
1991 ◽  
Vol 1 (4) ◽  
pp. 263-271 ◽  
Author(s):  
Jorge Bouzas ◽  
Floyd W. Bodyfelt ◽  
Antonio Torres

1979 ◽  
Vol 62 (3) ◽  
pp. 398-403 ◽  
Author(s):  
W.A. McGugan ◽  
D.B. Emmons ◽  
Elizabeth L. Armond
Keyword(s):  

2011 ◽  
Vol 94 (7) ◽  
pp. 3708-3714 ◽  
Author(s):  
B. Ganesan ◽  
C. Brothersen ◽  
D.J. McMahon

2004 ◽  
Vol 70 (8) ◽  
pp. 4814-4820 ◽  
Author(s):  
Jeffery R. Broadbent ◽  
Sanjay Gummalla ◽  
Joanne E. Hughes ◽  
Mark E. Johnson ◽  
Scott A. Rankin ◽  
...  

ABSTRACT Metabolism of aromatic amino acids by lactic acid bacteria is an important source of off-flavor compounds in Cheddar cheese. Previous work has shown that α-keto acids produced from Trp, Tyr, and Phe by aminotransferase enzymes are chemically labile and may degrade spontaneously into a variety of off-flavor compounds. However, dairy lactobacilli can convert unstable α-keto acids to more-stable α-hydroxy acids via the action of α-keto acid dehydrogenases such as d-hydroxyisocaproic acid dehydrogenase. To further characterize the role of this enzyme in cheese flavor, the Lactobacillus casei d-hydroxyisocaproic acid dehydrogenase gene was cloned into the high-copy-number vector pTRKH2 and transformed into L. casei ATCC 334. Enzyme assays confirmed that α-keto acid dehydrogenase activity was significantly higher in pTRKH2:dhic transformants than in wild-type cells. Reduced-fat Cheddar cheeses were made with Lactococcus lactis starter only, starter plus L. casei ATCC 334, and starter plus L. casei ATCC 334 transformed with pTRKH2:dhic. After 3 months of aging, the cheese chemistry and flavor attributes were evaluated instrumentally by gas chromatography-mass spectrometry and by descriptive sensory analysis. The culture system used significantly affected the concentrations of various ketones, aldehydes, alcohols, and esters and one sulfur compound in cheese. Results further indicated that enhanced expression of d-hydroxyisocaproic acid dehydrogenase suppressed spontaneous degradation of α-keto acids, but sensory work indicated that this effect retarded cheese flavor development.


1991 ◽  
Vol 74 (11) ◽  
pp. 3656-3668 ◽  
Author(s):  
C.L. Grazier ◽  
F.W. Bodyfelt ◽  
M.R. McDaniel ◽  
J.A. Torres

2016 ◽  
Vol 76 (2) ◽  
pp. 439-443 ◽  
Author(s):  
A. G. Moura ◽  
G. M. Santana ◽  
P. M. P. Ferreira ◽  
J. M. C. Sousa ◽  
A. P. Peron

Abstract Despite their great importance for the food industry, flavorings, in general, raise a number of questions regarding their cytotoxicity, mutagenicity and carcinogenicity, since, in the literature, there are few studies found evaluating the toxicity on the systemic and cellular level, of these chemical compounds. The root meristems of Allium cepa (onion) are widely used for the assessment of toxicity of chemical compounds of interest. Thus, this study aimed to evaluate, in A. cepa meristematic cells, individually and in combination at the cellular level, the toxicity of synthetic Cheese and Cheddar Cheese food flavorings, identical to the natural, at doses of 1.0 and 2.0 mL, at exposure times of 24 and 48 hours. In combination we used 0.5 mL of Cheese flavor associated with 0.5 mL of Cheddar flavor; and 1.0 mL of Cheese flavor associated with 1.0 mL of Cheddar flavor, at exposure times of 24 and 48 hours. For these evaluations, we used groups of five onion bulbs, which were first embedded in distilled water and then transferred to their respective doses. The root tips were collected and fixed in acetic acid (3:1) for 24 hours. The slides were prepared by crushing and were stained with 2% acetic orcein. Cells were analyzed throughout the cell cycle, totaling 5,000 for each control and exposure time. The mitotic indices calculated and cellular aberrations observed were subjected to statistical analysis using the chi-square test (p <0.05). No chromosomal abnormalities nor those of mitotic spindle were observed for the treatments performed. The results, both individually and in combination, showed that the flavorings under study significantly reduced the cell division rate of the test system cells used. Therefore, under the conditions studied, the two flavorings were cytotoxic.


1967 ◽  
Vol 50 (3) ◽  
pp. 292-297 ◽  
Author(s):  
T. Kristoffersen ◽  
E.M. Mikolajcik ◽  
I.A. Gould

Sign in / Sign up

Export Citation Format

Share Document