Alkaloids bacterial

Baitsch D, C Sandu, R Brandsch, GL Igloi (2001) Gene cluster on pAOl of Arthrobacter nicotinovorans involved in degradation of the plant alkaloid nicotine cloning, purification, and characterization of 2,6-dihydroxypyridine 3-hydrolase. J Bacterial 183 5262-5267. 

Kim SH, Shin DS, Oh MN, Chung SC, Lee JS, Oh KB. Inhibition of the bacterial surface protein anchoring transpeptidase sortase by isoquinoline alkaloids. Biosci Biotechnol Biochem 2004 68 421-424. 

Bacterial metabolites include novel alkaloids, peptides, and macrocyclic lactams. The most unusual metabolites from dmoflagellate are polyethers, both linear and macrolides. The latter were also found abundantly in brown seaweeds (Chart 7.6.FA/PO). Filamentous fimgi have afforded new isoindole and quinazoline alkaloids, as well as new-skeleton steroids (Chart 7.6.A/P/I). 

In green plants, which contain little or no cholesterol, cydoartenol is the key intermediate in sterol biosynthesis.161-1623 As indicated in Fig. 22-6, step c, cydoartenol can be formed if the proton at C-9 is shifted (as a hydride ion) to displace the methyl group from C-8. A proton is lost from the adjacent methyl group to close the cyclopropane ring. There are still other ways in which squalene is cyclized,162/163/1633 including some that incorporate nitrogen atoms and form alkaloids.1631 One pathway leads to the hop-anoids. These triterpene derivatives function in bacterial membranes, probably much as cholesterol does in our membranes. The three-dimensional structure of a bacterial hopene synthase is known.164 1643 Like glucoamylase (Fig. 2-29) and farnesyl transferase, the enzyme has an (a,a)6-barrel structure in one domain and a somewhat similar barrel in a second domain. 

Ellipticine inhibits DNA, RNA and protein synthesis. The inhibition is not reversible by removal of the alkaloid. It has no appreciable effects on thymidine and uridine kinases or on RNA polymerase, but it markedly inhibits DNA polymerase activity [240, 241]. The actual mechanism of action of ellipticine and related compounds has not yet been elucidated. Ellipticine and derivatives have been found to interact with bacterial membranes [242]. Many investigators have categorized these compounds as DNA-interacting or intercalating agents [230, 235, 237,243-246]. It has recently been postulated that mammalian DNA topoisomerase II may be a common target of these antitumour compounds [247],... 

Non-hemiterpenoid Quinolines.—A re-examination of the alkaloids of Haplophyllum dubium resulted in the isolation of two members of the 2-aryl-4-quinolone group, i.e. graveoline (2 R = Me) and the new alkaloid norgraveoline (2 R = H).5 A new bacterial pseudan (3) has been obtained from Pseudomonas aeruginosa.8... 

Aktories, K., Ed., Bacterial Toxins Tools in Cell Biology and Pharmacology, Chapman Hall, London, 1997. Alper, K.R. and Glick, S.D., Eds., The Alkaloids. Chemistry and Biology, Academic Press, San Diego, 2001. Dvorackova, I., Aflatoxins and Human Health, CRC Press, Boca Raton, FL, 1990. 

The families Catenicellidae and Flustridae produce alkaloids derived from tryptophan. The majority of these contain bromine at carbon 6 of the indole ring, although some are more extensively brominated. The convolutamydines (brominated tryptophan derivates isolated from the genus Amathia in the order Ctenostomata)128 are similarly brominated at carbon 6, suggesting a common biosynthetic pathway or bacterial symbiont. 

Tyski, S., Markiewicz, M., Gulewicz, K. and Twardowski, T. 1988. The effect of lupin alkaloids and ethanol extracts from seeds of Lupinus angustifolius on selected bacterial strains. J. Plant Physiol. 133, 240-242... 

WARZECHA, H GERASIMENKO, I., KUTCHAN, T.M., STOCKIGT, J., Molecular cloning and functional bacterial expression of a plant glucosidase specifically involved in alkaloid biosynthesis. Phytochemistry, 2000,54,657-666. 

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