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Featured researches published by D. J. Faulkner.


Cellular and Molecular Life Sciences | 1996

Two classes of metabolites from Theonella swinhoei are localized in distinct populations of bacterial symbionts.

C. A. Bewley; N. D. Holland; D. J. Faulkner

The marine spongeTheonella swinhoei (lithistid Family Theonellidae, Order Astrophorida) has yielded many important, bioactive natural products, most of which share structural features with bacterial natural products. The presence of microbial symbionts inT. swinhoei has been reported, and it was originally suggested that the cytotoxic macrolide swinholide A and many of the bioactive cyclic peptides fromT. swinhoei were all produced by symbiotic cyanobacteria. By transmission electron microscopy, we found four distinct cell populations to be consistently present inT. swinhoei: eukaryotic sponge cells, unicellular heterotrophic bacteria, unicellular cyanobacteria and filamentous heterotrophic bacteria. Purification and chemical analyses of each cell type showed the macrolide swinholide A to be limited to the mixed population of unicellular heterotrophic bacteria, and an anti-fungal cyclic peptide occurred only in the filamentous heterotrophic bacteria. Contrary to prior speculation, no major metabolites were located in the cyanobacteria or sponge cells.


Cellular and Molecular Life Sciences | 1989

Luffolide, a novel anti-inflammatory terpene from the sponge Luffariella sp.

M. R. Kernan; D. J. Faulkner; Parkanyi L; Jon Clardy; M. S. de Carvalho; Robert S. Jacobs

Luffolide (4) is a minor metabolite of the spongeLuffariella sp. from Palau. The structure of luffolide was determined by single crystal X-ray analysis. Luffolide is relatively unstable and undergoes a complex cyclization reaction to give the hexacyclic products5 and6. Luffolide (4) has some of the anti-inflammatory properties of manoalide (1): this may help to define the chemical reaction between manoalide (1) and phospholipase A2.


Journal of the American Chemical Society | 1976

A NOVEL DITERPENE FROM DOLLABELLA CALIFORNICA

Chris M. Ireland; D. J. Faulkner; Janet Finer; Jon Clardy


Molecular Pharmacology | 1989

Manoalide: structure-activity studies and definition of the pharmacophore for phospholipase A2 inactivation.

K B Glaser; M S de Carvalho; Robert S. Jacobs; M. R. Kernan; D. J. Faulkner


Journal of Organic Chemistry | 1987

The Luffariellins, novel antiinflammatory sesterterpenes of chemotaxonomic importance from the marine sponge Luffariella variabilis

M. R. Kernan; D. J. Faulkner; Robert S. Jacobs


Journal of the American Chemical Society | 1983

The denticulatins, two polypropionate metabolites from the pulmonate Siphonaria denticulata

Jill E. Hochlowski; D. J. Faulkner; Gayle K. Matsumoto; Jon Clardy


Journal of the American Chemical Society | 1973

Oppositol, a brominated sesquiterpene alcohol of a new skeletal class from the red alga, Laurencia subopposita

Hall Ss; D. J. Faulkner; Jose Fayos; Jon Clardy


Journal of the American Chemical Society | 1978

TRIDACHIONE, A PROPIONATE-DERIVED METABOLITE OF THE OPISTHOBRANCH MOLLUSC TRIDACHIELLA DIOMEDEA

Chris M. Ireland; D. J. Faulkner; Barbara A. Solheim; Jon Clardy


Journal of Organic Chemistry | 1983

Metabolites of the dorid nudibranch Chromodoris sedna

Jill E. Hochlowski; D. J. Faulkner; Lawrence S. Bass; Jon Clardy


Journal of the American Chemical Society | 1977

Trimethylenemethane. A reversible, temperature dependent transformation from higher to lower symmetry as observed by electron spin resonance spectroscopy.

Wratten Sj; D. J. Faulkner; Ken Hirotsu; Jon Clardy

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M. R. Kernan

University of California

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