Home LiteratureArticle Details
PMID: 7547886 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Effects of temperature and glycerides on the enhancement of Agkistrodon piscivorus piscivorus phospholipase A2 activity by lysolecithin and palmitic acid.

Biochemistry ·Vol. 34 ·No. 36 ·1995-09-12 ·Pages 11551-60

Bell JD, Baker ML, Bent ED, Ashton RW, Hemming DJ, Hansen LD

Abstract

The effect of temperature and various glycerides to modulate the ability of lysolecithin and fatty acid to promote high phospholipase A2 activity was studied using dipalmitoylphosphatidylcholine large unilamellar vesicles as substrate. The length of the lag phase prior to the accumulation of sufficient hydrolysis products (lysolecithin and fatty acid) to support high phospholipase activity was shortest at temperatures near the thermotropic phase transition of the phospholipid substrate. A reduction in the lag phase correlated with a reduction in the requirement for hydrolysis products at the phase transition temperature, where the bilayer exists in a state of fluctuating domains of gel and liquid crystal. Dipalmitoylglycerol and tripalmitoylglycerol also reduced the length of the lag phase. This reduction was both concentration-dependent and temperature-dependent relative to the phase transition in the presence of the glycerides. As with the effect of temperature, the ability of di- and triglycerides to decrease the lag time correlated with a decrease in the amount of reaction products necessary to promote high phospholipase activity. This effect coincided with the tendency of the glycerides to form domains in the bilayer. Glycerides that did not form domains either had no effect (monopalmitoylglycerol) or increased the length of the lag phase (dicaprylglycerol). These data suggest that the effect of the reaction products to increase phospholipase A2 activity is aided by the presence of fluctuations in lipid domains within the bilayer.

MeSH Terms
Agkistrodon Animals Calorimetry, Differential Scanning Crotalid Venoms/enzymology Energy Transfer Enzyme Activation Glycerides/pharmacology Group II Phospholipases A2 Hot Temperature Hydrolysis Kinetics Lysophosphatidylcholines/pharmacology Palmitic Acid Palmitic Acids/pharmacology Phospholipases A/drug effects,metabolism Phospholipases A2 Substrate Specificity
Chemicals
Crotalid Venoms Glycerides Lysophosphatidylcholines Palmitic Acids Palmitic Acid Phospholipases A Group II Phospholipases A2 Phospholipases A2
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bell J D
Department of Zoology, Brigham Young University, Provo, Utah 84602, USA.
Baker M L
Bent E D
Ashton R W
Hemming D J
Hansen L D
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1995-09-12
Pages
11551-60
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM49710 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]