Category:TP3

Revision as of 12:16, 9 August 2010

Triterpene (C30) Classes

Ring configuration

The basic structure is 4 carbon rings, cyclopenta[a]phenanthrene, gonane, or sterane. The rings B/C are always trans in all natural steroids. If the rings C/D are trans, it is called gonane. If its stereochemistry is unspecified, it is called sterane. Most steroids take gonane form, but in cardenolides and bufanolides, the rings C/D are cis.

Cyclopenta[a]phenanthrene	Gonane

The majority of steroids have methyl groups sticking out from the bridgehead positions C-10 and C-13. When these methyl groups (or hydrogens) stand above the plane, they are called β-configuration. Those below the plane are called α-configuration. If the configuration at any site is unknown, it is indicated as ξ (Greek Xi). By default, hydrogen atoms or substituents at the positions C-8, 9, 10, 13, and 14 are assumed to be 8β, 9α, 10β, 13β, and 14α configurations. C-5 is a special position, because there are as many 5α steroids as 5β are.

cholestane backbone	5α-configuration	5β-configuration

Biosynthesis

The starting point is squalene, which is formed by joining two FPPs tail-to-tail. Bacterial cyclases use squalene directly, but those of the other species use 2,3-oxidosqualene for cyclization.

• In bacteria, squalene is cyclized via the 17α-deoxydammarenyl cation to hopene and other triterpenes^[1].
• In eukaryotes, 2,3-oxidosqualene is cyclized via the protosteryl cation to lanosterol (animals and fungi) or cycloartenol (plants) by a series of 1,2-hydride and methyl shifts (Wagner-Meerwein shifts).^[2]
• In plants, various triterpenes arise from the dammarenyl cation.

ANIMALS, FUNGI, and YEAST	PLANTS
2,3-oxidosqualene
lanosterol synthase[3]				lupeol synthase
17β-protosteryl cation (C-B-C)[4]	1,2-shift	lanosteryl cation (C-C-C)		17β-dammarenyl cation (C-C-C)[5]
D-ring expansion      protostane		1,2-shift		D-ring expansion
unknown cation		lanostane cycloartane cucurbitane all steroids	baccharane	baccarenyl cation (C-C-C-C)
E-ring cyclization (from 18α)        E-ring cyclization (from 17β)			E-ring cyclization (from 18α)	E-ring   cyclization (from 18β)
hancolupyl cat. (C-B-C-C)	arborinyl cation (C-B-C-C)		H18β-lupyl cation (C-C-C-B)	H18α-lupyl cation (C-C-C-C)
1,2- shift	1,2- shift		1,2- shift	1,2- shift

1. ↑ Bacterial squalene cyclases can accept oxidosqualene as their substrates, but oxidosqualene usually does not exist in bacteria
2. ↑ A trace amount of phytosterols comes from lanosterol. Ohyama K, Suzuki M, Kikuchi J, Saito K, Muranaka T (2009) Dual biosynthetic pathways to phytosterol via cycloartenol and lanosterol in Arabidopsis Proc Natl Acad Sci USA 106(3):725-730
3. ↑ The most accessible enzyme among oxidosqualene cyclases.
   Ref. Corey EJ, Russey WE, Ortiz-de-Montellano PR (1966) 2,3-Oxidosqualene, an intermediate in the biological synthesis of sterols from squalene J Am Chem Soc 88:4750-1
4. ↑ The rings of protosteryl cation are chair-boat-chair configuration. The C-17 chain is β-configuration, not α.
   Ref. Corey EJ, Virgil SC (1991) An experimental demonstration of the stereochemistry of enzymic cyclization of 2,3-oxidosqualene to the protosterol system, forerunner of lanosterol and cholesterol. J Am Chem Soc 113:4025-6
5. ↑ The rings of dammarenyl cation are all-chair configuration. The C-17 chain is β-configuration.
   Ref. Xiong Q, Rocco F, Wilson WK, Xu R, Ceruti M, Matsuda SPT (2005) Structure and reactivity of the dammarenyl cation: configuration transmission in triterpene synthesis. J Org. Chem. 70:5362-75

Useful Reviews:

• Xu R, Fazio GC, Matsuda SPT (2004) On the origins of triterpenoid skeletal diversity. Phytochemstry 65:261-291 PMID 14751299

BACTERIA
squalene
squalene-hopene cyclase[1]
17α-deoxydammarenyl cation[2]
D-ring expansion[3]
hopene
Examples.

Design of Tri-terpene ID numbers ID番号の設計

x ... species information

y ... backbone structure (母核構造) 

Symbol at y	Carbons	Steroids	Backbone Structure
GN	C17	gonane
ES	C18	estrane
AD	C19	androstane
PG	C21	pregnane
CA	C24	cholane
CL	C27	cholestane
CM	C28	campestane
EG	C28	ergostane
SG	C29 (4 rings)	stigmastane
PR	C29 (4 rings)	poriferastane

Symbol at y	Carbons	Triterpenoids	Backbone Structure
PS	C30	protostane
EU	C30	euphane
LN	C30	lanostane
CY	C30	cycloartane
FS	C29	fusidane
HP	C30 (5 rings)	hopane
FN	C30 (5 rings)	fernane
CC	C30	cucurbitane
DM	C30	dammarane
BC	C30	baccharane
HL	C30	holostane
PF	C29 (5 rings)	pfaffane
LP	C30 (5 rings)	lupane
OL	C30 (5 rings)	oleanane
FD	C30 (5 rings)	friedelane
TR	C30 (5 rings)	taraxastane
UR	C30 (5 rings)	ursane
SR	C30 (5 rings)	serratane

r ... number of major rings (環構造数) 

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h ... hydroxylation pattern (水酸基数) 

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g ... glycosylation pattern(糖修飾パターン) 

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n ... number of sugars (修飾糖数) 

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c ... serial number (通し番号)