1995
DOI: 10.1007/bf00017482
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Localisation of the amathamide alkaloids in surface bacteria of Amathia wilsoni Kirkpatrick, 1888 (Bryozoa: Ctenostomata)

Abstract: The marine bryozoan Amathia wilsoni contains several brominated secondary metabolites, the alkaloid amathamides A-F. Energy dispersive X-ray analysis coupled with scanning electron microscopy was used to localise bromine in sections of Amathia wilsoni. Bromine concentrations higher than background levels were only found on the surface of the bryozoan and not within any of the different internal cell types . The correlation between bromine levels and a rod-shaped bacterium, ubiquitous to the tip region, points … Show more

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Cited by 21 publications
(13 citation statements)
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“…Bacterial biosynthesis of theopalauamide-type compounds is further corroborated by a study of Haygood, Faulkner and coworkers [50]. These include energy-dispersive X-ray analysis/scanning electron microscopy in the case of brominated natural products [34] and immunogold localization [40]. E. palauensis".…”
Section: Compound Localization Studiesmentioning
confidence: 82%
See 1 more Smart Citation
“…Bacterial biosynthesis of theopalauamide-type compounds is further corroborated by a study of Haygood, Faulkner and coworkers [50]. These include energy-dispersive X-ray analysis/scanning electron microscopy in the case of brominated natural products [34] and immunogold localization [40]. E. palauensis".…”
Section: Compound Localization Studiesmentioning
confidence: 82%
“…A number of research groups employed localization studies to obtain insights into biosynthetic sources [34][35][36][37][38][39][40][41][42][43][44][45][46]. Most exploited the property of sponges to dissociate into individual cells if they are transferred to artificial seawater lacking calcium and magnesium salts.…”
Section: Compound Localization Studiesmentioning
confidence: 99%
“…Quinone-tanned tube structures of polychaetes also contain haloaromatic amino acids (Vovelle et al 1994). Although the ultimate source of halometabolites from most marine organisms is not known, given the concentrations of halogenated products (PM-mM; Goerke , 1991, Higa et al 1987, Woodin et al 1993, Fielman & Targett 1995 and haloperoxidases (Ahern et al 1980, Chen et al 1991, Yoon et al 1994) and the currently observed presence of structurally diverse compounds among organisms collected from the same habitat, the most parsimonious explanation is that the worms themselves produce these compounds, unlike some sponge and bryozoan microbial associations where symbionts are the metabolite source (Unson et al 1994, Walls et al 1995.…”
Section: Discussionmentioning
confidence: 99%
“…Bacterial symbionts of eukaryotes often confer unique abilities that enable their host to survive on resources that would otherwise be unavailable. Examples include: chemoautotrophs (within the large worms, nematodes, bivalves and shrimp) living on sulfide or methane in a variety of marine habitats (Cary et al, 1997;Deming et al, 1997;Streams et al, 1997;Polz et al, 1998b;Fisher, 1990;Fujiwara et al, 2001); the production of toxins and antibiotics by bacteria (Kobayashi and Ishibashi, 1993;Faulkner et al, 1994;Walls et al, 1995;Kaufman et al, 1998;Currie, 1999;Davidson et al, 2001); the production of light (Hastings et al, 1987;Haygood, 1993); bacteria that degrade cellulose and fix nitrogen in shipworm bivalves and terrestrial termites to allow the hosts to live on wood (Breznak, 1982;Waterbury et al, 1983;Lilburn et al, 2001;Distel et al, 2002); and the associations of cyanobacteria with a variety of fungi to fix carbon and nitrogen (lichens). The activities of certain microbe-host associations, such as gut flora of termites and the nitrogen-fixing Rhizobium spp.…”
Section: The Metabolic Dimensionmentioning
confidence: 99%