Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry

Acyl-CoA:monoglyceride acyltransferase in microsomal preparations from the small intestine of the rat has been measured by means of continuous recording spectrophotometry. The reaction of 5,5′-dithiobis(2-nitrobenzoic acid) with CoA has been employed for this assay and optimal conditions for the rea...

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Main Author: John B. Rodgers, Jr.
Format: Article
Language:English
Published: Elsevier 1969-07-01
Series:Journal of Lipid Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520430718
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spelling doaj-929e8a215e7c4e04af42c5351b4c0f5b2021-04-24T05:55:18ZengElsevierJournal of Lipid Research0022-22751969-07-01104427432Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometryJohn B. Rodgers, Jr.0Department of Medicine (Gastroenterology), Albany Medical College, Albany, New York 12208Acyl-CoA:monoglyceride acyltransferase in microsomal preparations from the small intestine of the rat has been measured by means of continuous recording spectrophotometry. The reaction of 5,5′-dithiobis(2-nitrobenzoic acid) with CoA has been employed for this assay and optimal conditions for the reaction have been defined. One of the substrates, palmitoyl-CoA, inhibits the reaction even in modest concentrations. This inhibition is largely prevented by the addition of bovine serum albumin to the incubation medium. The reliability of the assay method was confirmed by comparison with the more cumbersome assay method that uses radioactive substrate.http://www.sciencedirect.com/science/article/pii/S0022227520430718small bowel mucosamicrosomal preparationsubstrate requirementssubstrate inhibitionbovine serum albuminnonionic detergent
collection DOAJ
language English
format Article
sources DOAJ
author John B. Rodgers, Jr.
spellingShingle John B. Rodgers, Jr.
Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
Journal of Lipid Research
small bowel mucosa
microsomal preparation
substrate requirements
substrate inhibition
bovine serum albumin
nonionic detergent
author_facet John B. Rodgers, Jr.
author_sort John B. Rodgers, Jr.
title Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
title_short Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
title_full Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
title_fullStr Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
title_full_unstemmed Assay of acyl-CoA:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
title_sort assay of acyl-coa:monoglyceride acyltransferase from rat small intestine using continuous recording spectrophotometry
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1969-07-01
description Acyl-CoA:monoglyceride acyltransferase in microsomal preparations from the small intestine of the rat has been measured by means of continuous recording spectrophotometry. The reaction of 5,5′-dithiobis(2-nitrobenzoic acid) with CoA has been employed for this assay and optimal conditions for the reaction have been defined. One of the substrates, palmitoyl-CoA, inhibits the reaction even in modest concentrations. This inhibition is largely prevented by the addition of bovine serum albumin to the incubation medium. The reliability of the assay method was confirmed by comparison with the more cumbersome assay method that uses radioactive substrate.
topic small bowel mucosa
microsomal preparation
substrate requirements
substrate inhibition
bovine serum albumin
nonionic detergent
url http://www.sciencedirect.com/science/article/pii/S0022227520430718
work_keys_str_mv AT johnbrodgersjr assayofacylcoamonoglycerideacyltransferasefromratsmallintestineusingcontinuousrecordingspectrophotometry
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