A non-extractable triterpenoid of the hopane series in Acetobacter xylinum
Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepent...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Herrmann, Dominique [verfasserIn] Bisseret, Philippe [verfasserIn] Connan, Jacques [verfasserIn] |
|---|
| Format: |
E-Artikel |
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| Erschienen: |
Oxford, UK: Blackwell Publishing Ltd ; 1996 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2006 ; Blackwell Publishing Journal Backfiles 1879-2005 |
|---|---|
| Übergeordnetes Werk: |
In: FEMS microbiology letters - Federation of European Microbiological Societies ; GKD-ID: 114439X, Oxford [u.a.] : Wiley-Blackwell, 1977, 135(1996), 2/3, Seite 0 |
| Übergeordnetes Werk: |
volume:135 ; year:1996 ; number:2/3 ; pages:0 |
| Links: |
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| DOI / URN: |
10.1111/j.1574-6968.1996.tb08008.x |
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NLEJ239783417 |
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| 520 | |a Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. | ||
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10.1111/j.1574-6968.1996.tb08008.x doi (DE-627)NLEJ239783417 DE-627 ger DE-627 rakwb Herrmann, Dominique verfasserin aut A non-extractable triterpenoid of the hopane series in Acetobacter xylinum Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Triterpenoids Bisseret, Philippe verfasserin aut Connan, Jacques verfasserin aut Rohmer, Michel oth In Federation of European Microbiological Societies ; GKD-ID: 114439X FEMS microbiology letters Oxford [u.a.] : Wiley-Blackwell, 1977 135(1996), 2/3, Seite 0 Online-Ressource (DE-627)NLEJ243927053 (DE-600)1501716-3 1574-6968 nnns volume:135 year:1996 number:2/3 pages:0 http://dx.doi.org/10.1111/j.1574-6968.1996.tb08008.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 135 1996 2/3 0 |
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10.1111/j.1574-6968.1996.tb08008.x doi (DE-627)NLEJ239783417 DE-627 ger DE-627 rakwb Herrmann, Dominique verfasserin aut A non-extractable triterpenoid of the hopane series in Acetobacter xylinum Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Triterpenoids Bisseret, Philippe verfasserin aut Connan, Jacques verfasserin aut Rohmer, Michel oth In Federation of European Microbiological Societies ; GKD-ID: 114439X FEMS microbiology letters Oxford [u.a.] : Wiley-Blackwell, 1977 135(1996), 2/3, Seite 0 Online-Ressource (DE-627)NLEJ243927053 (DE-600)1501716-3 1574-6968 nnns volume:135 year:1996 number:2/3 pages:0 http://dx.doi.org/10.1111/j.1574-6968.1996.tb08008.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 135 1996 2/3 0 |
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10.1111/j.1574-6968.1996.tb08008.x doi (DE-627)NLEJ239783417 DE-627 ger DE-627 rakwb Herrmann, Dominique verfasserin aut A non-extractable triterpenoid of the hopane series in Acetobacter xylinum Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Triterpenoids Bisseret, Philippe verfasserin aut Connan, Jacques verfasserin aut Rohmer, Michel oth In Federation of European Microbiological Societies ; GKD-ID: 114439X FEMS microbiology letters Oxford [u.a.] : Wiley-Blackwell, 1977 135(1996), 2/3, Seite 0 Online-Ressource (DE-627)NLEJ243927053 (DE-600)1501716-3 1574-6968 nnns volume:135 year:1996 number:2/3 pages:0 http://dx.doi.org/10.1111/j.1574-6968.1996.tb08008.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 135 1996 2/3 0 |
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10.1111/j.1574-6968.1996.tb08008.x doi (DE-627)NLEJ239783417 DE-627 ger DE-627 rakwb Herrmann, Dominique verfasserin aut A non-extractable triterpenoid of the hopane series in Acetobacter xylinum Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Triterpenoids Bisseret, Philippe verfasserin aut Connan, Jacques verfasserin aut Rohmer, Michel oth In Federation of European Microbiological Societies ; GKD-ID: 114439X FEMS microbiology letters Oxford [u.a.] : Wiley-Blackwell, 1977 135(1996), 2/3, Seite 0 Online-Ressource (DE-627)NLEJ243927053 (DE-600)1501716-3 1574-6968 nnns volume:135 year:1996 number:2/3 pages:0 http://dx.doi.org/10.1111/j.1574-6968.1996.tb08008.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 135 1996 2/3 0 |
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10.1111/j.1574-6968.1996.tb08008.x doi (DE-627)NLEJ239783417 DE-627 ger DE-627 rakwb Herrmann, Dominique verfasserin aut A non-extractable triterpenoid of the hopane series in Acetobacter xylinum Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. 2006 Blackwell Publishing Journal Backfiles 1879-2005 |2006|||||||||| Triterpenoids Bisseret, Philippe verfasserin aut Connan, Jacques verfasserin aut Rohmer, Michel oth In Federation of European Microbiological Societies ; GKD-ID: 114439X FEMS microbiology letters Oxford [u.a.] : Wiley-Blackwell, 1977 135(1996), 2/3, Seite 0 Online-Ressource (DE-627)NLEJ243927053 (DE-600)1501716-3 1574-6968 nnns volume:135 year:1996 number:2/3 pages:0 http://dx.doi.org/10.1111/j.1574-6968.1996.tb08008.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 135 1996 2/3 0 |
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Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. |
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Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. |
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Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. This is the first evidence of a probable selective complexation of a hopanoid via non-covalent linkages to other cell constituents. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ239783417</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707094206.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">120426s1996 xx |||||o 00| ||und c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1111/j.1574-6968.1996.tb08008.x</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ239783417</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Herrmann, Dominique</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">A non-extractable triterpenoid of the hopane series in Acetobacter xylinum</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Oxford, UK</subfield><subfield code="b">Blackwell Publishing Ltd</subfield><subfield code="c">1996</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Cells of the bacterium Acetobacter xylinum were analysed for their residual triterpenoid content after exhaustive lipid extraction using chloroform/methanol. Whereas the well known bacteriohopanetetrol mixture was present in the extract, the cells still contained a single bacteriohopanepentol cyclitol ether which could be detected either as the primary alcohol derivative after H5IO6 oxidation followed by NaBH4 reduction of the already extracted cells or as the octa-acetate by direct acetylation followed by solvent extraction. 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