Category:LBSB: Difference between revisions

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|style="background:lightgray"| <font size="+2">Sph<br/>d18:1</font>&nbsp;
|style="background:lightgray"| <font size="+2">Sph<br/>d18:1</font>&nbsp;
|Sph is an abbreviation of long-chain base. ''d''  or ''t'' stands for double, or triple hydroxy groups, respectively. (We count the terminal alcohol.)<br/>18 is the carbon chain length.<br/>1 is the number of unsaturated bonds (double bonds).
|Sph is an abbreviation of LCB.<br/>''d''  or ''t'' stands for double or triple hydroxy groups, respectively. (We count the terminal alcohol.)<br/>18 is the carbon chain length.<br/>1 after the colon is the number of unsaturated bonds (double bonds).
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Sphは長鎖塩基の略号。 ''d'', ''t'' はそれぞれ 2, 3 個の水酸基を意味する (アルコールの水酸基含む)。18は炭素鎖の長さ。1は不飽和結合(二重結合)の数。
Sphは長鎖塩基 LCB の略号。 ''d'', ''t'' はそれぞれ 2, 3 個の水酸基 (アルコールの水酸基含む)。18は炭素鎖長。コロンの次にくる1は不飽和結合(二重結合)の数。
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Revision as of 18:09, 15 March 2016


Upper classes: LB LBS

Long-chain base

Long-chain base (LCB or sphingoid base) is a 2-aminoalkane (or alkene) 1,3-diol. In cells, it constitutes sphingolipids and little exists as a free form. The structure varies depending on biological species

長鎖塩基 LCB(またはスフィンゴイド塩基)は 2-アミノアルカン(またはアルケン) 1,3-ジオールを指します。生体内ではスフィンゴ脂質の構成成分で、遊離のLCBは微量しか存在しません。生物種によってLCBの構造は大きく異なります。

Species
Higher animals C18 sphingosine (d18:1) [general]
d20:1 [nerve tissue], t18:0 [intestine]
Insects short-chain sphingosine (d14:1, d16:1) [general]
Plants (8E/Z)-d18:1, (8E/Z)-t18:1, (4E,8E/Z)-d18:2 [general]
Fungi 9-methyl (4E,8E)-d18:2, t18:0 [general]

Notation

Sph
d18:1
 
Sph is an abbreviation of LCB.
d or t stands for double or triple hydroxy groups, respectively. (We count the terminal alcohol.)
18 is the carbon chain length.
1 after the colon is the number of unsaturated bonds (double bonds).

Sphは長鎖塩基 LCB の略号。 d, t はそれぞれ 2, 3 個の水酸基 (アルコールの水酸基含む)。18は炭素鎖長。コロンの次にくる1は不飽和結合(二重結合)の数。

Major Sphingoid

Name Symbol Abbreviation Note
sphingosine = (4E)-sphingenine
(4E)-2-amino-octadec-4-ene-1,3-diol
d18:1 So Major in mammals
sphinganine = dihydrosphingosine
2-amino-octadecane-1,3-diol
d18:0 Sa or DHSo Lacking the trans-double bond of sphingosine
4-hydroxysphinganine = phytosphingosine
2-amino-octadecane-1,3,4-triol
t18:0 Phyto Major in fungi and plant
6-hydroxysphingosine
(4E)-2-amino-octadec-4-ene-1,3,6-triol
6-t18:1 Found in skin

Ceramides

The word ceramide (Cer) basically refers to all N-acyl-sphingoid bases, but most representative one is N-acylsphingosines. The conjugated fatty acids are often 16 to 26 carbon chains.

In mammalian skin, free ceramides comprise 55% of the intercellular lipid layer and exhibit barrier function. The ceramides may contain >30 carbon chains. Atopic dermatitis (and dry skin) is associated with a decrease and compositional change of such ceramides.

In industry, ceramides are extracted from vegetable-oil cakes from corn, rice, wheat, soybean, and others.

セラミドという言葉は基本的に N-アシルスフィンゴイド塩基を指すが、最も代表的なものは N-アシルスフィンゴシンである。結合する脂肪酸の炭素長は16から26である。

動物の皮膚における角質細胞間脂質では遊離のセラミドが55S%を占め、バリア機能を持つ。セラミドの長さも30以上に及ぶ。アトピー性皮膚炎や乾燥肌ではセラミド量が減少し、組成も変化していることが知られる。

工業的には、セラミドはトウモロコシ、コメ、コムギ、ダイズ等からの植物油滓から精製する。

Notation

Cer 
d18:1Δ8E/20:0
 
Cer is an abbreviations of ceramide. The first part indicates the sphingoid base and the second, after the slash, fatty acid.
In this website we do not use superscripts or subscripts for readability.
Also we do not italicize E (or trans) and Z (or cis) for the same reason.
Cerはセラミドの略号。左側が長鎖塩基、スラッシュを挟んで右側に脂肪酸。このサイトでは上付き/下付きは使用しない(見づらいため)。また E (トランス), Z (シス)もイタリックにしていない。

Composition

Species Glycosylceramide Glycosyl inositol phosphoceramide (GIPC)
Fatty acid Long chain base References Fatty acid Long chain base References
Plants h16:0 - h26:0
h16:1 - h26:1
h16:0
VLCFA
d18:2Δ4E8E/Z
d18:2Δ4E8E/Z
d18:1Δ8E/Z
t18:1Δ8E/Z
[1][2]
[1][2]
[1]
[1][2]
hVLCFA
h14:0 - h26:0
h20:1 - h26:1
t18:1Δ8E/Z
t18:1Δ8E/Z, t18:0
t18:1Δ8E/Z, t18:0
[1]
[3]
[1][3]
Fungi h16:0 - h18:0
h16:1 - h18:1
9-methyl d18:2Δ4E,8E
9-methyl d18:2Δ4E,8E
[4][2]
[4][2]
h24:0 - h26:0
h24:1 - h26:1
h16:0 - h26:0
t18:0
t18:0
t18:0, t20:0
[4]
[2]
[2][3]
  1. 1.0 1.1 1.2 1.3 1.4 1.5 Markham JE, Lynch DV, Napier JA, Dunn TM, Cahoon EB. Plant sphingolipids: function follows form. Curr Opin Plant Biol. 2013 16: 350-7. doi: 10.1016/j.pbi.2013.02.009.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 Warnecke D, Heinz E..Recently discovered functions of glucosylceramides in plants and fungi. Cell Mol Life Sci. 2003 60:919-41.doi: 10.1007/s00018-003-2243-4.
  3. 3.0 3.1 3.2 Buré C, Cacas JL, Mongrand S, Schmitter JM. Characterization of glycosyl inositol phosphoryl ceramides from plants and fungi by mass spectrometry. Anal Bioanal Chem. 2013 doi: 10.1007/s00216-013-7130-8.
  4. 4.0 4.1 4.2 Nimrichter L, Rodrigues ML. Fungal glucosylceramides: from structural components to biologically active targets of new antimicrobials. Front Microbiol. 2011 2:212. doi: 10.3389/fmicb.2011.00212.

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