Bacterial hopanoids from pink-pigmented facultative methylotrophs (PPFMs) and from green plant surfaces

References

1. Bisseret P., Zundel M., Rohmer M. 1985; Prokaryotic triterpenoids 2β-Methylhopanoids from Methylobacterium organophilum and Nostoc muscorum a new series of prokaryotic triterpenoids. Eur J Biochem 150:29–34
   [Google Scholar]
2. Bousfield I.J., Green P.N. Reclassification of bacteria of the genus Protomonas (Urikami and Komagata, 1984) in the genus Methylobacterium (Platt, Cole and Hanson) Emend Green and Bousfield, 1985. Int J Syst Bacteriol 1985; 35:209
   [Google Scholar]
3. Corpe W.A. A method for detecting methylotrophic bacteria on solid surfaces. J Microbiol Methods 1985; 3:215–221
   [Google Scholar]
4. Corpe W.A., Basile D.V. Methanol-utilizing bacteria associated with green plants. Dev Ind Microbiol 1982; 23:483–493
   [Google Scholar]
5. Corpe W.A., Jensen T.E. Major antigens in Methylobacterium species and their location in cells using immunoelectron microscopic methods. Cytobios 1991; 67:117–126
   [Google Scholar]
6. Corpe W.A., Rheem S. Ecology of the methylotrophic bacteria on living leaf surfaces. FEMS Microbiol Ecol 1989; 62:243–250
   [Google Scholar]
7. Corpe W.A., Jensen T.E., Baxter M. Fine structure of cytoplasmic inclusions of some methylotrophic bacteria from plant surfaces. Arch Microbiol 1986; 145:107–112
   [Google Scholar]
8. Flesch G., Rohmer M. A novel hopanoid from the ethanol-producing bacterium Zymomonas mobilis. Biochem J 1986; 262:673–675
   [Google Scholar]
9. Flesch G., Rohmer M. Prokaryotic hopanoids: the biosynthesis of the bacteriohopane skeleton Formation of isoprenic units from two distinct acetate pools and a novel type of carbon/carbon linkage between a triterpene and D-ribose. Eur J Biochem 1988; 175:405–411
   [Google Scholar]
10. Green P.N., Bousfield I.J. A taxonomic study of some Gram-negative facultatively methylotrophic bacteria. J Gen Microbiol 1982; 128:623–638
    [Google Scholar]
11. Green P.N., Bousfield I.J. Emendation of Methylobacterium (Patt, Cole and Hanson, 1976); Methylobacterium rhodium (Heumann, 1962). comb. nov. corrig; Methylobacterium radiotolerans (Ito and Izuha, 1971) comb. nov. corrig., and Methylobacterium mesophilicum (Austin and Goodfellow, 1979) comb. nov.. Int J Syst Bacteriol 1983; 33:875–878
    [Google Scholar]
12. Green P.N., Bousfield I.J., Hood D. Three new Methylobacterium species: M. rhodesianum sp. nov., M. zatmanii sp. nov., M. fujisawaense sp. nov. Int J Syst Bacteriol 1988; 38:124–127
    [Google Scholar]
13. Hestrin S., Schramm M. The synthesis of cellulose by Acetobacter xylinum. Biochem J 1954; 58:345–352
    [Google Scholar]
14. Hood D.W., Dow C.S., Green P.N. DNA:DNA hybridization studies of the pink-pigmented, facultative methylotrophs. J Gen Microbiol 1987; 133:709–720
    [Google Scholar]
15. Jürgens U.V., Simonin P., Rohmer M. Localization and distribution of hopanoids in membrane systems of the cyano-bacterium Synechocystis PCC 6714. FEMS Microbiol Lett 1992; 92:85–288
    [Google Scholar]
16. Marsili A., Morelli I., Bernardin C., Pacchiani M. onstituents of some mosses. Phytochemistry 1972; 11:2003–2005
    [Google Scholar]
17. Ourisson G., Albrecht P., Rohmer M. The hopanoids, paleochemistry and biochemistry of a group of natural products. Pure Appl Chem 1979; 51:709–729
    [Google Scholar]
18. Peiseler B., Rohmer M. Prokaryotic triterpenoids. (22R,32R)-34-35-Dinorbacteriohopane-32,33-diols from Acetobacter aceti ssp xylinum: new bacteriohopane derivatives with shortened side-chain.. J Chem Soc Perkin 1991; I:2449–2453
    [Google Scholar]
19. Renoux J.M., Rohmer M. Prokaryotic triterpenoids: new bacteriohopanetetrol cyclitol ethers from the methylotrophic bacterium Methylobacterium organophilum. Eur J Biochem 1985; 151:405–410
    [Google Scholar]
20. Rohmer M., Ourisson G. Unsaturated bacteriohopanepolyols from Acetobacter aceti ssp. xylinum. J Chem Res (S) 356 1986; 357:3037–3059
    [Google Scholar]
21. Rohmer M., Bouvier-Nave P., Ourisson G. Distribution of hopanoid triterpenes in prokaryotes. J Gen Microbiol 1984; 130:1137–1150
    [Google Scholar]
22. Rohmer M., Sutter B., Sahm H. Bacterial sterol surrogates. Biosynthesis of the side-chain of bacteriohopanetrol and of a carbocyclic carbapseudopentose from 13C labelled glucose in Zymomonas mobilis. J Chem Soc Chem Commun 19891471–1472
    [Google Scholar]
23. Rohmer M., Knani M., Simonin P., Sutter B., Sahm H. soprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate. Biochem J 1993; 295:517–524
    [Google Scholar]
24. Schwencker U., Onge M.S., Gingras G. Chemical and physical properties of a carotenoprotein from Rhodospirillum rubrum. Biochim Biophys Acta 1974; 351:246–260
    [Google Scholar]
25. Simonin P. 1993 Nouvelle voie de biosynthèse des isoprènoϊtdes chez les bactèries. Biohopanoϊtdes bactèriens Thèse, Universitè de Haute Alsace; Mulhouse, France: nnn 0,1-2
    [Google Scholar]
26. Stampf P., Herrmann D., Bisseret P., Rohmer M. 2α-Methylhopanoids: first recognition in the bacterium Methylobacterium organophilum and obtention via sulphur induced isomerization of 2β-methylhopanoids. Tetrahedron 1991; 34:7081–7090
    [Google Scholar]
27. Thirkell D., Hunter M.I.S. Carotenoid-glycoprotein of Sarcina flava membrane. J Gen Microbiol 1969; 58:289–292
    [Google Scholar]
28. Zundel M., Rohmer M. Prokaryotic triterpenoids: 3β-methylhopanoids from Acetobacter species and Methylococcus cap-sulatus. Eur J Biochem 1985; 150:23–27
    [Google Scholar]