Chemistry:Juvabione

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Juvabione
Juvabione.svg
Names
Preferred IUPAC name
Methyl (4R)-4-[(2R)-6-methyl-4-oxoheptan-2-yl]cyclohex-1-ene-1-carboxylate
Identifiers
3D model (JSmol)
ChemSpider
Properties
C16H26O3
Molar mass 266.381 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Juvabione, historically known as the paper factor, is the methyl ester of todomatuic acid. Both are sesquiterpenes (C15) found in the wood of true firs of the genus Abies.[1][2][3][4][5][6][7] They occur naturally as part of a mixture of sesquiterpenes based upon the bisabolane scaffold. Sesquiterpenes of this family are known as insect juvenile hormone analogues (IJHA) because of their ability to mimic juvenile activity in order to stifle insect reproduction and growth.[3] These compounds play important roles in conifers as the second line of defense against insect induced trauma and fungal pathogens.[3][4]

JH3, Juvabione, Todo.png

History

In 1965, Karel Sláma and Carroll Williams made a surprising discovery: paper towels made from the wood of the balsam fir (Abies balsamea, Fig. 1) released vapors that elicited a potent effect on hemipteran bugs of the Pyrrhocoridae family.[1][2] They named this substance "the paper factor." It was thought to contain a mixture of JH-mimicking sesquiterpenes, but it wasn't until 1966 that (+)-juvabione was first isolated as an active component from the balsam fir by Bowers.[2]

Abies balsamea.jpg

Figure 1. Abies balsamea

Induction of sesquiterpene biosynthesis in conifers

Insect herbivores such as bark beetles and their symbiotic fungal pathogens, pose as one of the greatest threats to conifer survival. When they feed on conifers, the subsequent wounds trigger a signaling cascade that results in the production of terpene synthases of many types,[lower-alpha 1] all of which arise from the terpene synthase gene cluster known as Tpsd.[4] Induced gene expression is tightly regulated and time-dependent. Immediately after insect attack, toxic monoterpenes are released. These provide a volatile solvent for the diterpene resins so that successive evaporation leaves a barrier that seals the wound site.[5]

The transcription of sesquiterpene synthases was shown to begin on the third day following insect attack. Sesquiterpenoid JHAs continue to be produced up to twelve days later to prevent further insect reproduction.[5] The first sesquiterpene to be formed, (E)-α-bisabolene (formed by (E)-α-bisabolene synthase), can be further transformed into juvabione and todomatuic acid.[3][4]

Biosynthesis of (+)-juvabione and (+)-todomatuic acid

Sesquiterpenes are a class of terpenoids based upon a 15-carbon unit scaffold synthesized from isoprene units via the mevalonate pathway (Fig. 2). In this pathway,[6][8] two molecules of acetyl-CoA undergo a condensation reaction to give acetoacetyl-CoA. This product then condenses with third molecule of acetyl-CoA in a stereospecific fashion to form 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) which then is reduced to mevalonic acid (MVA). A series of ATP-dependent transformations lead to a key isoprene unit, isopentenyl diphosphate (IPP) which can be isomerized to dimethylallyl diphosphate (DMAPP). DMAPP ionizes to its respective allylic cation that undergoes electrophilic addition to the double bond of IPP.[9] Upon loss of a proton, geranyl diphosphate (GPP) is formed. GPP undergoes an elimination reaction to form its corresponding allylic cation. Electrophilic addition of another IPP unit to the GPP cation results in a tertiary carbocation intermediate that forms a fifteen-carbon farnesyl diphosphate (FPP) upon loss of a proton.

MVA pathway.png

Figure 2. Generalized pathway for the synthesis of sesquiterpenes.

Farnesyl diphosphate is the universal precursor to a wide variety of linear and cyclized sesquiterpenes. Of particular interest to juvabione biosynthesis (Scheme 1), dissociation of the terminal diphosphate from the FPP precursor generates the (E,E)-farnesyl allylic cation, leading to nerolidyl diphosphate (NPP). NPP is another precursor that can undergo different reaction types, but in this case, bisabolene synthase directs a single cyclization event by electrophilic attack of C-1 onto the double bond of C-6 to form a six-membered ring. Deprotonation of the resultant tertiary cation yields (E)-α-bisabolene. Currently, the mechanistic details describing the conversion of (E)-α-bisabolene to (+)-juvabione and (+)-todomatuic acid have not been fully described.

Juvabione biosynthetic pathway.png

Scheme 1. Biosynthetic pathway for the synthesis of juvabione and todomatuic acid from FPP precursor.

Notes

  1. ↑ Examples include: Myrcene synthase, pinene synthase, and taxadiene synthase

References

  1. ↑ 1.0 1.1 Manville, J. F.; Kriz, C. D. (1977). "Juvabione and its analogues. IV. Isolation, identification, and occurrence of juvabione, juvabiol, epijuvabiol from the whole wood of Abies lasiocarpa". Can. J. Chem. 55: 2547–2553. doi:10.1139/v77-351. 
  2. ↑ 2.0 2.1 2.2 Manville, J. F. (1975). "Juvabione and its analogues. Juvabione and delta4'-dehydrojuvabione isolated from the whole wood of Abies balsamea, have the R>R stereoconfigurations, not R,S". Can. J. Chem. 53: 1579–1585. doi:10.1139/v75-223. 
  3. ↑ 3.0 3.1 3.2 3.3 Bohlmann, J.; Crock, J.; Jetter, R.; Croteau, R. (1998). "Terpenoid-based defenses in conifers: cDNA cloning, characterization, and functional expression of wound-inducible (E)-alpha-bisabolene synthase from grand fir (Abies grandis)". Proc. Natl. Acad. Sci. USA 95 (12): 6756–6761. doi:10.1073/pnas.95.12.6756. PMID 9618485. Bibcode: 1998PNAS...95.6756B. 
  4. ↑ 4.0 4.1 4.2 4.3 Phillips, M. A; Bohlmann, J.; Gershenzon, J. (2006). "Molecular regulation of induced terpenoid biosynthesis in conifers". Phytochemistry Reviews 55 (5): 179–189. doi:10.1007/s11101-006-0001-6. 
  5. ↑ 5.0 5.1 5.2 Bohlmann, J.; Meyer-Gauen, G.; Croteau, R. (1998). "Plant terpenoid synthases: Molecular biology and phylogenetic analysis". Proc. Natl. Acad. Sci. USA 95 (8): 4126–4133. doi:10.1073/pnas.95.8.4126. PMID 9539701. Bibcode: 1998PNAS...95.4126B. 
  6. ↑ 6.0 6.1 Steele, C. L.; Crock, J.; Bohlmann, J.; Croteau, R. (1998). "Sesquiterpene Synthases from Grand Fir (Abies grandis)". J. Biol. Chem. 273 (4): 2078–2089. doi:10.1074/jbc.273.4.2078. PMID 9442047. 
  7. ↑ Higuchi, T. (1985). Biosynthesis and biodegradation of wood components. Academic Press. pp. 380–429. 
  8. ↑ Dewick, P. M (2009). "The mevalonate and methylerythritol phosphate pathways: terpenoids and steroids". Medicinal Natural Products, 3rd Edition; Wiley: United Kingdom: 187–234. doi:10.1002/9780470742761.ch5. ISBN 9780470742761. 
  9. ↑ Cane, David E.; Abell, Christopher; Harrison, Paul H. M.; Hubbard, Brian R.; Kane, Charles T.; Lattman, Rene; Oliver, John S.; Weiner, Steven W. (1991). "Terpenoid Biosynthesis and the Stereochemistry of Enzyme-Catalysed Allylic Addition-Elimination Reactions". Philosophical Transactions: Biological Sciences 332 (1263): 123–129. ISSN 0962-8436. https://www.jstor.org/stable/55545. 



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