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DOI10.1007/s10973-014-4171-y
Enhancement effect of solutes of low molecular mass on the insect antifreeze protein ApAFP752 from Anatolica polita
Liu, Zhongyuan1; Li, Honglei2; Pang, Hai3; Ma, Ji1; Mao, Xinfang1
通讯作者Mao, Xinfang
来源期刊JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
ISSN1388-6150
EISSN1572-8943
出版年2015
卷号120期号:1页码:307-315
英文摘要

Many ectotherms produce antifreeze proteins (AFPs), also known as thermal hysteresis proteins that can lower non-colligatively freezing point of body liquids without altering the melting point. The difference between the depressed freezing point and the melting point, termed thermal hysteresis (TH), is usually a measure of the antifreeze activity of AFPs. Certain low molecular mass molecules and proteins can further enhance the antifreeze activity of AFPs. The enhancement effects of several salts, polycarboxylates, and polyhydroxy compounds on an antifreeze protein (ApAFP752) from the desert beetle Anatolica polita were determined using differential scanning calorimetry. These observations suggest that the salts including NaCl, KCl, CaCl2, and MgCl2 can enhance colligatively the thermal hysteresis activity (THA) of ApAFP752. The bivalent ions were more effective than monovalent ions at low concentrations. The enhancing effects of three polycarboxylates were higher than that of the neutral salts, and the more carboxylate groups per enhancer molecule the better the efficiency of the enhancer. Ethylenediaminetetraacetic acid disodium salt showed the strongest synergism ability and increased the THA nearly 13-fold from 0.45 A degrees C in its absence to 5.67 A degrees C. Glycerol and trehalose, the polyhydroxy compounds studied, had limited enhancement efficiency on ApAFP752, and only enhance the TH of the protein at high concentration. Mechanisms are discussed.


英文关键词Antifreeze proteins Thermal hysteresis activity DSC Enhancers
类型Article
语种英语
国家Peoples R China
收录类别SCI-E
WOS记录号WOS:000352139800038
WOS关键词BEETLE DENDROIDES-CANADENSIS ; WINTER FLOUNDER ANTIFREEZE ; BINDING MECHANISM ; ICE ; HYSTERESIS ; TOLERANCE ; DSC ; GLYCOPROTEINS ; INHIBITION ; BACTERIA
WOS类目Thermodynamics ; Chemistry, Analytical ; Chemistry, Physical
WOS研究方向Thermodynamics ; Chemistry
来源机构新疆大学 ; 清华大学
资源类型期刊论文
条目标识符http://119.78.100.177/qdio/handle/2XILL650/189017
作者单位1.Xinjiang Univ, Coll Life Sci & Technol, Xinjiang Key Lab Biol Resources & Genet Engn, Urumqi 830046, Peoples R China;
2.Zhengzhou Tourism Coll, Zhengzhou 450009, Peoples R China;
3.Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China
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Liu, Zhongyuan,Li, Honglei,Pang, Hai,et al. Enhancement effect of solutes of low molecular mass on the insect antifreeze protein ApAFP752 from Anatolica polita[J]. 新疆大学, 清华大学,2015,120(1):307-315.
APA Liu, Zhongyuan,Li, Honglei,Pang, Hai,Ma, Ji,&Mao, Xinfang.(2015).Enhancement effect of solutes of low molecular mass on the insect antifreeze protein ApAFP752 from Anatolica polita.JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY,120(1),307-315.
MLA Liu, Zhongyuan,et al."Enhancement effect of solutes of low molecular mass on the insect antifreeze protein ApAFP752 from Anatolica polita".JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY 120.1(2015):307-315.
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