Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds.

alpha-Cyclodextrin at concentrations of 1–8 mM helps dissolve, in aqueous solution, fatty acids such as lignoceric, stearic, and palmitic, and complex lipids such as ceramide and cerebroside that contain these acids. Formation of an inclusion complex was indicated on examination of the solution by g...
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Gespeichert in:

Autor*in:	I Singh [verfasserIn] Y Kishimoto [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	1983

Übergeordnetes Werk:	In: Journal of Lipid Research - Elsevier, 2021, 24(1983), 5, Seite 662-665
Übergeordnetes Werk:	volume:24 ; year:1983 ; number:5 ; pages:662-665

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1016/S0022-2275(20)37973-6

Katalog-ID:	DOAJ05488327X

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author	I Singh
spellingShingle	I Singh misc QD415-436 misc Biochemistry Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds.
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topic_title	QD415-436 Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds
topic	misc QD415-436 misc Biochemistry
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title	Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds.
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title_full	Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds
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title_sort	effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds
callnumber	QD415-436
title_auth	Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds.
abstract	alpha-Cyclodextrin at concentrations of 1–8 mM helps dissolve, in aqueous solution, fatty acids such as lignoceric, stearic, and palmitic, and complex lipids such as ceramide and cerebroside that contain these acids. Formation of an inclusion complex was indicated on examination of the solution by gel filtration. alpha-Cyclodextrin strikingly increased synthesis of ceramide from sphingosine and either free lignoceric or stearic acid by rat brain preparations. These results suggest the further use of alpha-cyclodextrin in lipid enzymology, especially in relation to sphingolipid metabolism.
abstractGer	alpha-Cyclodextrin at concentrations of 1–8 mM helps dissolve, in aqueous solution, fatty acids such as lignoceric, stearic, and palmitic, and complex lipids such as ceramide and cerebroside that contain these acids. Formation of an inclusion complex was indicated on examination of the solution by gel filtration. alpha-Cyclodextrin strikingly increased synthesis of ceramide from sphingosine and either free lignoceric or stearic acid by rat brain preparations. These results suggest the further use of alpha-cyclodextrin in lipid enzymology, especially in relation to sphingolipid metabolism.
abstract_unstemmed	alpha-Cyclodextrin at concentrations of 1–8 mM helps dissolve, in aqueous solution, fatty acids such as lignoceric, stearic, and palmitic, and complex lipids such as ceramide and cerebroside that contain these acids. Formation of an inclusion complex was indicated on examination of the solution by gel filtration. alpha-Cyclodextrin strikingly increased synthesis of ceramide from sphingosine and either free lignoceric or stearic acid by rat brain preparations. These results suggest the further use of alpha-cyclodextrin in lipid enzymology, especially in relation to sphingolipid metabolism.
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title_short	Effect of cyclodextrins on the solubilization of lignoceric acid, ceramide, and cerebroside, and on the enzymatic reactions involving these compounds.
url	https://doi.org/10.1016/S0022-2275(20)37973-6 https://doaj.org/article/fe6f7aac88a142b0ae4cd942f9ea6ada http://www.sciencedirect.com/science/article/pii/S0022227520379736 https://doaj.org/toc/0022-2275
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