terpenes
TRANSCRIPT
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Terpenes are the building blocks for a number of molecules
Phytol tail on chlorophyllUbiquinone tailGibberellinsCytokininSteroidsMany secondary products
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Terpenes are the building blocks for a number of molecules
Phytol tail on chlorophyllUbiquinone tailGibberellinsCytokininSteroidsMany secondary products
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Fig. 24.01
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Fig. 24.02Terpenes are made from C5 units
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Fig. 24.03
Thyme leaf surface Spearmint trichome
Secretory cavity lemon Resin duct, Jeffrey Pine
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Nuts and Bolts
The terpene lecture is on the webPapers are due Thursday, May 9Final exam Saturday, May 18 - 105 Tureaud
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Terpenes are the building blocks for a number of molecules
Phytol tail on chlorophyllUbiquinone tailGibberellinsCytokininSteroidsMany secondary products
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In plants, hemes are built from glutamate in the chloroplast
In animals and fungi, hemes are made from succinyl CoA and glycine in the mitochondria
The chlorophyll phytol tail is a terpene
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Fig. 12.04phytol
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Succinyl CoA + glycine
Heme Biosynthesis (animals)
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Fig. 12.05
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Glutamic acid to ALA
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Two ALA molecules are condensed to make porphobilinogen
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Fig. 12.05
4 porphobilinogen molecules make up protoporphyrinogen IX
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Fig. 12.05
Chlorophyll biosynthesis begins with chelation of Mg+2
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Fig. 12.05
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Chlorophyll biosynthetic intermediates
Protoporphyrinogen – four ringsProtochlorophyllide – Ring V is madeChlorophyllide – Ring IV is reduced Chlorophyll – phytol is atttached
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Terpenes are the building blocks for a number of molecules
Phytol tail on chlorophyllUbiquinone tailGibberellinsCytokininSteroidsMany secondary products
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The isoprene unit is the basic building block of terpenes
The isoprene unit has five carbons
Three Acetyl CoA molecules make up mevalonic acid (MVA) which has (6 carbons)MVA is oxidized, CO2 is lost and isopentenylpyrophosphate (IPP) is made
This occurs in the ERThere is another pathway in the plastid (don’t worry about it)
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Fig. 24.04
ER pathway
Highly regulated
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Fig. 24.04
ER pathway(continued)
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Fig. 24.05
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Fig. 14.25 Plastid pathway (top)
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Fig. 24.07
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Yes
No
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Fig. 12.07
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Fig. 12.08
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C20
C40
head to head dimerization
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Fig. 17.24
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Fig. 17.27
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See also Figure 17.28
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Fig. 17.61
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Fig. 17.62
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Fig. 17.05
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Fig. 17.08
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Fig. 17.09
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Fig. 17.12
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Fig. 17.32
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Fig. 17.35
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Monoterpenes
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Sesquiterpenes
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Diterpenes
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