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Volumn 46, Issue 3, 2011, Pages 249-261

N-acylated bacteriohopanehexol-mannosamides from the thermophilic bacterium Alicyclobacillus acidoterrestris

Author keywords

Cyclohexyl fatty acids; Alicyclobacillus acidoterrestris; Circular dichroism; N Acylated bacteriohopanehexol mannosamides; Negative RP HPLC ESI MS MS

Indexed keywords

BACTERIOHOPANE; BACTERIOHOPANEPOLYOL; HOPANOID; N ACYLATED BACTERIOHOPANEHEXOL MANNOSAMIDE DERIVATIVE; PENTACYCLIC TRITERPENE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79955934956     PISSN: 00244201     EISSN: 15589307     Source Type: Journal    
DOI: 10.1007/s11745-010-3482-4     Document Type: Article
Times cited : (18)

References (44)
  • 1
    • 0031925117 scopus 로고    scopus 로고
    • Analysis of bacteriohopanepolyols in sediment and bacterial extracts by high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry
    • DOI 10.1002/(SICI)1097-0231(19980529)12:10<609::AID-RCM210>3.0. CO;2-U
    • Fox PA, Carter J, Farrimond P (1998) Analysis of bacteriohopanepolyols in sediment and bacterial extracts by high performance liquid chromatography/ atmospheric pressure chemical ionization mass spectrometry. Rapid Commun Mass Spectrom 12:609-612 (Pubitemid 28222702)
    • (1998) Rapid Communications in Mass Spectrometry , vol.12 , Issue.10 , pp. 609-612
    • Fox, P.A.1    Carter, J.2    Farrimond, P.3
  • 2
    • 34547116444 scopus 로고    scopus 로고
    • Bacterial populations recorded in diverse sedimentary biohopanoid distributions
    • DOI 10.1016/j.orggeochem.2007.04.006, PII S014663800700099X
    • Talbot HM, Farrimond P (2007) Bacterial populations recorded in diverse sedimentary biohopanoid distributions. Org Geochem 38:1212-1225 (Pubitemid 47102429)
    • (2007) Organic Geochemistry , vol.38 , Issue.8 , pp. 1212-1225
    • Talbot, H.M.1    Farrimond, P.2
  • 3
    • 0000730062 scopus 로고
    • Hopanoids. 2. Biohopanoids: A novel class of bacterial lipids
    • Ourisson G, Rohmer M (1992) Hopanoids. 2. Biohopanoids: a novel class of bacterial lipids. Acc Chem Res 25:403-408
    • (1992) Acc Chem Res , vol.25 , pp. 403-408
    • Ourisson, G.1    Rohmer, M.2
  • 4
    • 0032943554 scopus 로고    scopus 로고
    • Hopanoid biosynthesis and function in bacteria
    • DOI 10.1007/s001140050592
    • Kannenberg EL, Poralla K (1999) Hopanoid biosynthesis and function in bacteria. Naturwissenschaften 86:168-176 (Pubitemid 29200204)
    • (1999) Naturwissenschaften , vol.86 , Issue.4 , pp. 168-176
    • Kannenberg, E.L.1    Poralla, K.2
  • 5
    • 33947274082 scopus 로고    scopus 로고
    • Rapid structural elucidation of composite bacterial hopanoids by atmospheric pressure chemical ionisation liquid chromatography/ion trap mass spectrometry
    • DOI 10.1002/rcm.2911
    • Talbot HM, Rohmer M, Farrimond P (2007) Rapid structural elucidation of composite bacterial hopanoids by atmospheric pressure chemical ionisation liquid chromatography/ion trap mass spectrometry. Rapid Commun Mass Spectrom 21:880-892 (Pubitemid 46426807)
    • (2007) Rapid Communications in Mass Spectrometry , vol.21 , Issue.6 , pp. 880-892
    • Talbot, H.M.1    Rohmer, M.2    Farrimond, P.3
  • 6
    • 0032118776 scopus 로고    scopus 로고
    • Surface active behavior of hopanoid lipids: Bacteriohopanetetrol and phenylacetate monoester bacteriohopanetetrol
    • Stroeve P, Pettit CD, Vasquez V, Kim I, Berry AM (1998) Surface active behavior of hopanoid lipids: bacteriohopanetetrol and phenylacetate monoester bacteriohopanetetrol. Langmuir 14:4261-4265 (Pubitemid 128624896)
    • (1998) Langmuir , vol.14 , Issue.15 , pp. 4261-4265
    • Stroeve, P.1    Pettit, C.D.2    Vasquez, V.3    Kim, I.4    Berry, A.M.5
  • 7
    • 0033677898 scopus 로고    scopus 로고
    • Bacteriohopanehexol, a new triterpene from the marine sponge Petrosia species
    • Shatz M, Yosief T, Kashman Y (2000) Bacteriohopanehexol, a new triterpene from the marine sponge Petrosia species. J Nat Prod 63:1554-1556
    • (2000) J Nat Prod , vol.63 , pp. 1554-1556
    • Shatz, M.1    Yosief, T.2    Kashman, Y.3
  • 8
    • 0001692419 scopus 로고
    • The biosynthesis of triterpenoids of the hopane series in the eubacteria: A mine of new enzyme reactions
    • Rohmer M (1993) The biosynthesis of triterpenoids of the hopane series in the eubacteria: a mine of new enzyme reactions. Pure Appl Chem 65:1293-1298
    • (1993) Pure Appl Chem , vol.65 , pp. 1293-1298
    • Rohmer, M.1
  • 9
    • 0034595620 scopus 로고    scopus 로고
    • The first 12-methylhopanoid: 12-Methylbacteriohopanetetrol from the marine sponge Plakortis simplex
    • PII S0040402000003045
    • Costantino V, Fattorusso E, Imperatore C, Mangoni A (2000) The first 12-methylhopanoid: 12-methylbacteriohopanetetrol from the marine sponge Plakortis simplex. Tetrahedron 56:3781-3784 (Pubitemid 30354129)
    • (2000) Tetrahedron , vol.56 , Issue.23 , pp. 3781-3784
    • Costantino, V.1    Fattorusso, E.2    Imperatore, C.3    Mangoni, A.4
  • 10
    • 34948877661 scopus 로고    scopus 로고
    • Diastereoselective synthesis of aminobacteriohopanetetrol, a biomarker for methanotrophic bacteria: Confirmation of the absolute configuration
    • DOI 10.1002/cbdv.200790175
    • Pan W, Zhang Y, Liang G, Rohmer M, Sinay P, Vincent SP (2007) Diastereoselective synthesis of aminobacteriohopanetetrol, a biomarker for methanotrophic bacteria: confirmation of the absolute configuration. Chem Biodivers 4:2182-2189 (Pubitemid 47527669)
    • (2007) Chemistry and Biodiversity , vol.4 , Issue.9 , pp. 2182-2189
    • Pan, W.1    Zhang, Y.2    Liang, G.3    Rohmer, M.4    Sinay, P.5    Vincent, S.P.6
  • 11
    • 0026659141 scopus 로고
    • 35-O-β-6-amino-6-deoxyglucopyranosyl bacteriohopanetetrol, a novel triterpenoid of the hopane series from the cyanobacterium Synechocystis SP PCC-6714
    • Simonin P, Jurgens UJ, Rohmer M (1992) 35-O-β-6-amino-6- deoxyglucopyranosyl bacteriohopanetetrol, a novel triterpenoid of the hopane series from the cyanobacterium Synechocystis SP PCC-6714. Tetrahedron Lett 33:3629-3632
    • (1992) Tetrahedron Lett , vol.33 , pp. 3629-3632
    • Simonin, P.1    Jurgens, U.J.2    Rohmer, M.3
  • 12
    • 0030045628 scopus 로고    scopus 로고
    • A non-extractable triterpenoid of the hopane series in Acetobacter xylinum
    • DOI 10.1016/0378-1097(95)00473-4
    • Herrmann D, Bisseret P, Connan J, Rohmer M (1996) A nonextractable triterpenoid of the hopane series in Acetobacter xylinum. FEMS Microbiol Lett 135:323-326 (Pubitemid 26051669)
    • (1996) FEMS Microbiology Letters , vol.135 , Issue.2-3 , pp. 323-326
    • Herrmann, D.1    Bisseret, P.2    Connan, J.3    Rohmer, M.4
  • 13
    • 1542331424 scopus 로고    scopus 로고
    • Influence of the temperature and the growth phase on the hopanoids and fatty acids content of Frateuria aurantia (DSMZ 6220)
    • DOI 10.1016/S0168-6496(03)00302-7, PII S0168649603003027
    • Joyeux C, Fouchard S, Llopiz P, Neunlist S (2004) Influence of the temperature and the growth phase on the hopanoids and fatty acids content of Frateuria aurantia (DSMZ 6220). FEMS Microbiol Ecol 47:371-379 (Pubitemid 38296613)
    • (2004) FEMS Microbiology Ecology , vol.47 , Issue.3 , pp. 371-379
    • Joyeux, C.1    Fouchard, S.2    Llopiz, P.3    Neunlist, S.4
  • 14
    • 0022395551 scopus 로고
    • Novel hopanoids from the methylotrophic bacteria Methylococcus capsulatus and Methylomonas methanica. (22S)-35-aminobacteriophane-30,31, 32,33,34-pentol and (22S)-35-amino-3b-methylbacteriophane-30,31,32,33,34-pentol
    • Neunlist S, Rohmer M (1985) Novel hopanoids from the methylotrophic bacteria Methylococcus capsulatus and Methylomonas methanica. (22S)-35-aminobacteriophane-30, 31, 32, 33, 34-pentol and (22S)-35-amino-3b- methylbacteriophane-30, 31, 32, 33, 34-pentol. Biochem J 231:635-639 (Pubitemid 16194557)
    • (1985) Biochemical Journal , vol.231 , Issue.3 , pp. 635-639
    • Neunlist, S.1    Rohmer, M.2
  • 15
    • 0033986814 scopus 로고    scopus 로고
    • Bacterial triterpenoids of the hopane series from the methanotrophic bacteria Methylocaldum spp.: Phylogenetic implications and first evidence for an unsaturated aminobacteriohopanepolyol
    • DOI 10.1016/S0378-1097(99)00610-2, PII S0378109799006102
    • Cvejic JH, Bodrossy L, Kovacs KL, Rohmer M (2000) Bacterial triterpenoids of the hopane series from the methanotrophic bacteria Methylocaldum spp.: phylogenetic implications and first evidence for an unsaturated aminobacteriohopanepolyol. FEMS Microbiol Lett 182:361-365 (Pubitemid 30006932)
    • (2000) FEMS Microbiology Letters , vol.182 , Issue.2 , pp. 361-365
    • Cvejic, J.H.1    Bodrossy, L.2    Kovacs, K.L.3    Rohmer, M.4
  • 16
    • 39149088291 scopus 로고    scopus 로고
    • Cyanobacterial bacteriohopanepolyol signatures from cultures and natural environmental settings
    • Talbot HM, Summons RE, Jahnke LL, Cockell CS, Rohmer M, Farrimond P (2008) Cyanobacterial bacteriohopanepolyol signatures from cultures and natural environmental settings. Org Geochem 39:232-263
    • (2008) Org Geochem , vol.39 , pp. 232-263
    • Talbot, H.M.1    Summons, R.E.2    Jahnke, L.L.3    Cockell, C.S.4    Rohmer, M.5    Farrimond, P.6
  • 17
    • 49149110335 scopus 로고    scopus 로고
    • Bacterial populations recorded in bacteriohopanepolyol distributions in soils from Northern England
    • Cooke MP, Talbot HM, Farrimond P (2008) Bacterial populations recorded in bacteriohopanepolyol distributions in soils from Northern England. Org Geochem 39:1347-1358
    • (2008) Org Geochem , vol.39 , pp. 1347-1358
    • Cooke, M.P.1    Talbot, H.M.2    Farrimond, P.3
  • 18
    • 58149267975 scopus 로고    scopus 로고
    • Fatty acids, unusual glycophospholipids and DNA analyses of thermophilic bacteria isolated from hot springs
    • Siristova L, Melzoch K, Rezanka T (2009) Fatty acids, unusual glycophospholipids and DNA analyses of thermophilic bacteria isolated from hot springs. Extremophiles 13:101-109
    • (2009) Extremophiles , vol.13 , pp. 101-109
    • Siristova, L.1    Melzoch, K.2    Rezanka, T.3
  • 19
    • 67349258264 scopus 로고    scopus 로고
    • Identification of (S)-11-cycloheptyl-4-methylundecanoic acid in acylphosphatidylglycerol from Alicyclobacillus acidoterrestris
    • Rezanka T, Siristova L, Melzoch K, Sigler K (2009) Identification of (S)-11-cycloheptyl-4-methylundecanoic acid in acylphosphatidylglycerol from Alicyclobacillus acidoterrestris. Chem Phys Lipids 158:104-113
    • (2009) Chem Phys Lipids , vol.158 , pp. 104-113
    • Rezanka, T.1    Siristova, L.2    Melzoch, K.3    Sigler, K.4
  • 20
    • 69849105178 scopus 로고    scopus 로고
    • Direct ESI-MS analysis of O-acyl glycosylated cardiolipins from the thermophilic bacterium Alicyclobacillus acidoterrestris
    • Rezanka T, Siristova L, Melzoch K, Sigler K (2009) Direct ESI-MS analysis of O-acyl glycosylated cardiolipins from the thermophilic bacterium Alicyclobacillus acidoterrestris. Chem Phys Lipids 161:115-121
    • (2009) Chem Phys Lipids , vol.161 , pp. 115-121
    • Rezanka, T.1    Siristova, L.2    Melzoch, K.3    Sigler, K.4
  • 21
    • 33845261493 scopus 로고
    • A rapid method of total lipid extraction and purification
    • Bligh EG, Dyer WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37:911-917
    • (1959) Can J Biochem Physiol , vol.37 , pp. 911-917
    • Bligh, E.G.1    Dyer, W.J.2
  • 22
    • 0028835809 scopus 로고
    • Analysis of intact hopanoids and other lipids from the bacterium Zymomonas mobilis by high-performance liquid chromatography
    • Moreau RA, Powell MJ, Osman SF, Whitaker BD, Fett WF, Roth L, O'Brien DJ (1995) Analysis of intact hopanoids and other lipids from the bacterium Zymomonas mobilis by high-performance liquid chromatography. Anal Biochem 224:293-301
    • (1995) Anal Biochem , vol.224 , pp. 293-301
    • Moreau, R.A.1    Powell, M.J.2    Osman, S.F.3    Whitaker, B.D.4    Fett, W.F.5    Roth, L.6    O'Brien, D.J.7
  • 23
    • 0025313438 scopus 로고
    • Identification of very long polyenoic acids as picolinyl esters by Ag ion-exchange high-performance liquid chromatography, reversed-phase high-performance liquid chromatography
    • Rezanka T (1990) Identification of very long polyenoic acids as picolinyl esters by Ag ion-exchange high-performance liquid chromatography, reversed-phase high-performance liquid chromatography. J Chromatogr 513:344-348
    • (1990) J Chromatogr , vol.513 , pp. 344-348
    • Rezanka, T.1
  • 24
    • 0141940656 scopus 로고    scopus 로고
    • The economical synthesis of [20-13C, 1,3-15N2]uridine; preliminary conformational studies by solid state NMR
    • Patching SG, Middleton DA, Henderson PJF, Herbert RB (2003) The economical synthesis of [20-13C, 1,3-15N2]uridine; preliminary conformational studies by solid state NMR. Org Biomol Chem 1:2057-2062
    • (2003) Org Biomol Chem , vol.1 , pp. 2057-2062
    • Patching, S.G.1    Middleton, D.A.2    Henderson, P.J.F.3    Herbert, R.B.4
  • 25
    • 0000490375 scopus 로고
    • D-talose anomerization: NMR methods to evaluate the reaction kinetics
    • Snyder JR, Johnston ER, Serianni AS (1989) D-talose anomerization: NMR methods to evaluate the reaction kinetics. J Amer Chem Soc 111:2681-2687
    • (1989) J Amer Chem Soc , vol.111 , pp. 2681-2687
    • Snyder, J.R.1    Johnston, E.R.2    Serianni, A.S.3
  • 26
    • 34250435033 scopus 로고
    • Monosaccharides - Communication 26. β-methyl-D-alloheptopyranoside- 4-ulose and syntheses based on it
    • Dmitriev BA, Chernyak AYa, Chizhov OS, Kochetkov NK (1972) Monosaccharides - communication 26. β-methyl-D-alloheptopyranoside-4-ulose and syntheses based on it. Russ Chem B 21:2230-2235
    • (1972) Russ Chem B , vol.21 , pp. 2230-2235
    • Dmitriev, B.A.1    Chernyak, A.Ya.2    Chizhov, O.S.3    Kochetkov, N.K.4
  • 27
    • 0034680677 scopus 로고    scopus 로고
    • Homologation of protected hexoses with Grignard C1 reagents
    • Kim M, Grzeszczyk B, Zamojski A (2000) Homologation of protected hexoses with Grignard C1 reagents. Tetrahedron 56:9319-9337
    • (2000) Tetrahedron , vol.56 , pp. 9319-9337
    • Kim, M.1    Grzeszczyk, B.2    Zamojski, A.3
  • 28
    • 0007055107 scopus 로고
    • D-glycero-D-allo-Heptose, L-allo-Heptulose, D-talo-Heptulose and related substances derived from the addition of cyanide to D-allose
    • Pratt JW, Richtmyer NK (1955) D-glycero-D-allo-Heptose, L-allo-Heptulose, D-talo-Heptulose and related substances derived from the addition of cyanide to D-allose. J Amer Chem Soc 77:6326-6328
    • (1955) J Amer Chem Soc , vol.77 , pp. 6326-6328
    • Pratt, J.W.1    Richtmyer, N.K.2
  • 29
    • 84970619320 scopus 로고
    • Equilibria between pyranoses and furanoses. 5. The composition in solution and the C-13 NMR-spectra of the heptoses and the heptuloses
    • Angyal SJ, Tran TQ (1983) Equilibria between pyranoses and furanoses. 5. The composition in solution and the C-13 NMR-spectra of the heptoses and the heptuloses. Aust J Chem 36:937-946
    • (1983) Aust J Chem , vol.36 , pp. 937-946
    • Angyal, S.J.1    Tran, T.Q.2
  • 30
    • 0026716536 scopus 로고
    • Synthesis of a branched-chain inosose derivative, a versatile synthon of N-substituted valiolamine derivatives from D-glucose
    • Fukase H, Horii S (1992) Synthesis of a branched-chain inosose derivative, a versatile synthon of N-substituted valiolamine derivatives from D-glucose. J Org Chem 57:3642-3650
    • (1992) J Org Chem , vol.57 , pp. 3642-3650
    • Fukase, H.1    Horii, S.2
  • 31
    • 0035083535 scopus 로고    scopus 로고
    • Novel methylated triterpenoids of the gammacerane series from the nitrogen-fixing bacterium Bradyrhizobium japonicum USDA 110
    • DOI 10.1046/j.1432-1327.2001.01998.x
    • Bravo J-M, Perzl M, Hartner T, Kannenberg EL, Rohmer M (2001) Novel methylated triterpenoids of the gammacerane series from the nitrogen-fixing bacterium Bradyrhizobium japonicum USDA 110. Eur J Biochem 268:1323-1331 (Pubitemid 32231885)
    • (2001) European Journal of Biochemistry , vol.268 , Issue.5 , pp. 1323-1331
    • Bravo, J.-M.1    Perzl, M.2    Hartner, T.3    Kannenberg, E.L.4    Rohmer, M.5
  • 32
    • 0345505746 scopus 로고    scopus 로고
    • Atmospheric pressure chemical ionisation reversed-phase liquid chromatography/ion trap mass spectrometry of intact bacteriohopanepolyols
    • DOI 10.1002/rcm.974
    • Talbot HM, Squier AH, Keely BJ, Farrimond P (2003) Atmospheric pressure chemical ionisation reversed-phase liquid chromatography/ion trap mass spectrometry of intact bacteriohopanepolyols. Rapid Commun Mass Spectrom 17:728-737 (Pubitemid 36373175)
    • (2003) Rapid Communications in Mass Spectrometry , vol.17 , Issue.7 , pp. 728-737
    • Talbot, H.M.1    Squier, A.H.2    Keely, B.J.3    Farrimond, P.4
  • 33
    • 23044453132 scopus 로고    scopus 로고
    • Concise syntheses of bacteriohopanetetrol and its glucosamine derivative
    • DOI 10.1039/b504558d
    • Pan W, Zhang Y, Liang G, Vincent SP, Sinay P (2005) Concise syntheses of bacteriohopanetetrol and its glucosamine derivative. Chem Commun 27:3445-3447 (Pubitemid 41059076)
    • (2005) Chemical Communications , Issue.27 , pp. 3445-3447
    • Pan, W.1    Zhang, Y.2    Liang, G.3    Vincent, S.P.4    Sinay, P.5
  • 34
    • 0001168053 scopus 로고
    • Carbon-13 NMR study of a- and b-anomeric pairs of D-mannopyranosides and L-rhamnopyranosides
    • Kasai R, Okihara M, Asakawa J, Mizutani K, Tanaka O (1979) Carbon-13 NMR study of a- and b-anomeric pairs of D-mannopyranosides and L-rhamnopyranosides. Tetrahedron 35:1427-1432
    • (1979) Tetrahedron , vol.35 , pp. 1427-1432
    • Kasai, R.1    Okihara, M.2    Asakawa, J.3    Mizutani, K.4    Tanaka, O.5
  • 35
    • 0000792452 scopus 로고
    • Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: Synthesis of both enantiomers of high-carbon monosaccharides
    • Lin C-H, Sugai T, Halcomb RL, Ichikawa Y, Wong C-H (1992) Unusual stereoselectivity in sialic acid aldolase-catalyzed aldol condensations: synthesis of both enantiomers of high-carbon monosaccharides. J Amer Chem Soc 114:10138-10145
    • (1992) J Amer Chem Soc , vol.114 , pp. 10138-10145
    • Lin, C.-H.1    Sugai, T.2    Halcomb, R.L.3    Ichikawa, Y.4    Wong, C.-H.5
  • 36
    • 0023952382 scopus 로고
    • Practical syntheses of immunologically relevant β-glycosides of 2-acetamido-2-deoxy-D-mannopyranose. Methyl N-acetyl-β-D-mannosaminide, N-acetyl-β-D-mannosaminyl-(1 → 6)-D-galactose, and methyl N-acetyl-β-D-mannosaminyl-(1 → 4)-α-D-glucopyranoside
    • Kaji E, Lichtenthaler FW, Nishino T, Yamane A, Zen S (1988) Practical syntheses of immunologically relevant β-glycosides of 2-acetamido-2-deoxy- D-mannopyranose. Methyl N-acetyl-β-D-mannosaminide, N-acetyl-β-D- mannosaminyl-(1 → 6)-D-galactose, and methyl N-acetyl-β-D- mannosaminyl-(1 → 4)-α-D-glucopyranoside. Bull Chem Soc Jpn 61:1291-1297
    • (1988) Bull Chem Soc Jpn , vol.61 , pp. 1291-1297
    • Kaji, E.1    Lichtenthaler, F.W.2    Nishino, T.3    Yamane, A.4    Zen, S.5
  • 37
    • 0001195845 scopus 로고
    • Bacterial sterol surrogates. Determination of the absolute configuration of bacteriohopanetetrol side chain by hemisynthesis of its diastereoisomers
    • Bisseret P, Rohmer M (1989) Bacterial sterol surrogates. Determination of the absolute configuration of bacteriohopanetetrol side chain by hemisynthesis of its diastereoisomers. J Org Chem 54:2958-2964
    • (1989) J Org Chem , vol.54 , pp. 2958-2964
    • Bisseret, P.1    Rohmer, M.2
  • 39
    • 0027442036 scopus 로고
    • Assignment of relative and absolute configuration of acyclic polyols and aminopolyols by circular dichroism-trends follow Fischer's sugar family tree
    • Zhou P, Berova N, Wiesler WT, Nakanishi K (1993) Assignment of relative and absolute configuration of acyclic polyols and aminopolyols by circular dichroism-trends follow Fischer's sugar family tree. Tetrahedron 49:9343-9352
    • (1993) Tetrahedron , vol.49 , pp. 9343-9352
    • Zhou, P.1    Berova, N.2    Wiesler, W.T.3    Nakanishi, K.4
  • 40
    • 0030057553 scopus 로고    scopus 로고
    • Structures of two bacteriohopanoids with acyclic pentol side-chains from the cyanobacterium Nostoc PCC 6720
    • DOI 10.1016/0040-4020(96)00013-0
    • Zhao N, Berova N, Nakanishi K, Rohmer M, Mougenot P, Jurgens UJ (1996) Structures of two bacteriohopanoids with acyclic pentol side-chains from the cyanobacterium Nostoc PCC 6720. Tetrahedron 52:2777-2788 (Pubitemid 26060087)
    • (1996) Tetrahedron , vol.52 , Issue.8 , pp. 2777-2788
    • Zhao, N.1    Berova, N.2    Nakanishi, K.3    Rohmer, M.4    Mougenot, P.5    Jurgens, U.J.6
  • 41
    • 0001573068 scopus 로고
    • Microscale CD method for determining absolute configurations of acyclic amino tetrols and amino pentols. Structures of aminobacteriohopanepolyols from the methylotrophic bacterium Methylococcus luteus
    • Zhou P, Berova N, Nakanishi K, Knani M, Rohmer M (1991) Microscale CD method for determining absolute configurations of acyclic amino tetrols and amino pentols. Structures of aminobacteriohopanepolyols from the methylotrophic bacterium Methylococcus luteus. J Amer Chem Soc 113:4040-4041
    • (1991) J Amer Chem Soc , vol.113 , pp. 4040-4041
    • Zhou, P.1    Berova, N.2    Nakanishi, K.3    Knani, M.4    Rohmer, M.5
  • 42
    • 37049079861 scopus 로고
    • Assignment of absolute stereochemistry of aminopolyols by the bichromophoric exciton chirality method
    • Zhou P, Berova N, Nakanishi K, Rohmer M (1991) Assignment of absolute stereochemistry of aminopolyols by the bichromophoric exciton chirality method. J Chem Soc Chem Commun, pp 256-258
    • (1991) J Chem Soc Chem Commun , pp. 256-258
    • Zhou, P.1    Berova, N.2    Nakanishi, K.3    Rohmer, M.4
  • 43
    • 0000205970 scopus 로고
    • A simple spectroscopic method for assigning relative and absolute configuration in acyclic 1, 2, 3-triols
    • Wiesler WT, Nakanishi K (1989) A simple spectroscopic method for assigning relative and absolute configuration in acyclic 1, 2, 3-triols. J Amer Chem Soc 111:3446-3447
    • (1989) J Amer Chem Soc , vol.111 , pp. 3446-3447
    • Wiesler, W.T.1    Nakanishi, K.2
  • 44
    • 0029973224 scopus 로고    scopus 로고
    • Bacterial triterpenoids of the hopane series from the prochlorophyte Prochlorothrix hollandica and their intracellular localization
    • Simonin P, Jurgens UJ, Rohmer M (1996) Bacterial triterpenoids of the hopane series from the prochlorophyte Prochlorothrix hollandica and their intracellular localization. Eur J Biochem 241:865-871 (Pubitemid 26379390)
    • (1996) European Journal of Biochemistry , vol.241 , Issue.3 , pp. 865-871
    • Simonin, P.1    Jurgens, U.J.2    Rohmer, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.