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1. (CSDB ID: 50985) | report error |
| Subst-(1-5)-Subst-(1-5)-Subst-(1-5)-Subst-(1-6)-D-Man-ol Subst = 3,5-dihydroxydecanoic acid = SMILES CCCCC{5}C(O)C{3}C(O)C{1}C(O)=O | Show graphically |
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Aureobasidium pullulans NRRL62031
(Ancestor NCBI TaxID 5580,
species name lookup)
uni-muenster.deLiamocins are a class of biosurfactants with growing interest. However, methods for identification and quantification of liamocins on the molecular level are lagging behind. Therefore, we developed a chromatographic separation based on supercritical fluid chromatography (SFC) for liamocins and structurally related exophilins. The different congeners could be separated on a charge modulated hydroxyethyl amide functionalized silica-based column. Coupling to high-resolution mass spectrometry (MS) revealed four exophilin species and four liamocin species with mannitol and arabitol as polyol head group in a sample of the yeast-like fungus Aureobasidium pullulans (A. pullulans). In contrast to a recently published reversed phase high-performance liquid chromatography (HPLC) method, the different subclasses (exophilins, mannitol liamocins and arabitol liamocins) were additionally separated by means of SFC. The structures were confirmed by their accurate masses and tandem mass spectrometry (MS/MS). A complementary quantification method was developed using SFC coupled to charged-aerosol detection (CAD) to overcome the disadvantages of quantification by means of MS without authentic standards. A flow compensation by varying the make-up flow was used to obtain a constant composition of the mobile phase during detection and to ensure a stable detector response. The concentrations of the individual liamocin species were determined using an external calibration with n-octyl-β-D-glycopyranoside. The total amount of these concentrations agrees with the dry weight of an aliquot of the heavy oil. The developed SFC-based method has the advantage of shorter analysis time and superior selectivity compared to the previously published LC separation. In brief, the here presented SFC hyphenations enable comprehensive analysis of liamocin biosurfactants providing identification and absolute quantification of individual congeners.
glycolipids, biosurfactants, high-resolution mass spectrometry, liamocins, charged-aerosol detection, supercritical fluid chromatography
Structure type: monomer ; 949.5703|
2. (CSDB ID: 50986) | report error |
| Subst-(1-5)-Subst-(1-5)-Subst3Ac-(1-6)-D-Man-ol Subst = 3,5-dihydroxydecanoic acid = SMILES CCCCC{5}C(O)C{3}C(O)C{1}C(O)=O | Show graphically |
|
Show legend Show as text |
Aureobasidium pullulans NRRL62031
(Ancestor NCBI TaxID 5580,
species name lookup)
uni-muenster.deLiamocins are a class of biosurfactants with growing interest. However, methods for identification and quantification of liamocins on the molecular level are lagging behind. Therefore, we developed a chromatographic separation based on supercritical fluid chromatography (SFC) for liamocins and structurally related exophilins. The different congeners could be separated on a charge modulated hydroxyethyl amide functionalized silica-based column. Coupling to high-resolution mass spectrometry (MS) revealed four exophilin species and four liamocin species with mannitol and arabitol as polyol head group in a sample of the yeast-like fungus Aureobasidium pullulans (A. pullulans). In contrast to a recently published reversed phase high-performance liquid chromatography (HPLC) method, the different subclasses (exophilins, mannitol liamocins and arabitol liamocins) were additionally separated by means of SFC. The structures were confirmed by their accurate masses and tandem mass spectrometry (MS/MS). A complementary quantification method was developed using SFC coupled to charged-aerosol detection (CAD) to overcome the disadvantages of quantification by means of MS without authentic standards. A flow compensation by varying the make-up flow was used to obtain a constant composition of the mobile phase during detection and to ensure a stable detector response. The concentrations of the individual liamocin species were determined using an external calibration with n-octyl-β-D-glycopyranoside. The total amount of these concentrations agrees with the dry weight of an aliquot of the heavy oil. The developed SFC-based method has the advantage of shorter analysis time and superior selectivity compared to the previously published LC separation. In brief, the here presented SFC hyphenations enable comprehensive analysis of liamocin biosurfactants providing identification and absolute quantification of individual congeners.
glycolipids, biosurfactants, high-resolution mass spectrometry, liamocins, charged-aerosol detection, supercritical fluid chromatography
Structure type: monomer ; 805.4551|
3. (CSDB ID: 50987) | report error |
| Subst-(1-5)-Subst-(1-5)-Subst-(1-5)-Subst-(1-5)-Ara-ol Subst = 3,5-dihydroxydecanoic acid = SMILES CCCCC{5}C(O)C{3}C(O)C{1}C(O)=O | Show graphically |
|
Show legend Show as text |
Aureobasidium pullulans NRRL62031
(Ancestor NCBI TaxID 5580,
species name lookup)
uni-muenster.deLiamocins are a class of biosurfactants with growing interest. However, methods for identification and quantification of liamocins on the molecular level are lagging behind. Therefore, we developed a chromatographic separation based on supercritical fluid chromatography (SFC) for liamocins and structurally related exophilins. The different congeners could be separated on a charge modulated hydroxyethyl amide functionalized silica-based column. Coupling to high-resolution mass spectrometry (MS) revealed four exophilin species and four liamocin species with mannitol and arabitol as polyol head group in a sample of the yeast-like fungus Aureobasidium pullulans (A. pullulans). In contrast to a recently published reversed phase high-performance liquid chromatography (HPLC) method, the different subclasses (exophilins, mannitol liamocins and arabitol liamocins) were additionally separated by means of SFC. The structures were confirmed by their accurate masses and tandem mass spectrometry (MS/MS). A complementary quantification method was developed using SFC coupled to charged-aerosol detection (CAD) to overcome the disadvantages of quantification by means of MS without authentic standards. A flow compensation by varying the make-up flow was used to obtain a constant composition of the mobile phase during detection and to ensure a stable detector response. The concentrations of the individual liamocin species were determined using an external calibration with n-octyl-β-D-glycopyranoside. The total amount of these concentrations agrees with the dry weight of an aliquot of the heavy oil. The developed SFC-based method has the advantage of shorter analysis time and superior selectivity compared to the previously published LC separation. In brief, the here presented SFC hyphenations enable comprehensive analysis of liamocin biosurfactants providing identification and absolute quantification of individual congeners.
glycolipids, biosurfactants, high-resolution mass spectrometry, liamocins, charged-aerosol detection, supercritical fluid chromatography
Structure type: monomer ; 919.5604|
4. (CSDB ID: 50988) | report error |
| Subst-(1-5)-Subst-(1-5)-Subst3Ac-(1-5)-Ara-ol Subst = 3,5-dihydroxydecanoic acid = SMILES CCCCC{5}C(O)C{3}C(O)C{1}C(O)=O | Show graphically |
|
Show legend Show as text |
Aureobasidium pullulans NRRL62031
(Ancestor NCBI TaxID 5580,
species name lookup)
uni-muenster.deLiamocins are a class of biosurfactants with growing interest. However, methods for identification and quantification of liamocins on the molecular level are lagging behind. Therefore, we developed a chromatographic separation based on supercritical fluid chromatography (SFC) for liamocins and structurally related exophilins. The different congeners could be separated on a charge modulated hydroxyethyl amide functionalized silica-based column. Coupling to high-resolution mass spectrometry (MS) revealed four exophilin species and four liamocin species with mannitol and arabitol as polyol head group in a sample of the yeast-like fungus Aureobasidium pullulans (A. pullulans). In contrast to a recently published reversed phase high-performance liquid chromatography (HPLC) method, the different subclasses (exophilins, mannitol liamocins and arabitol liamocins) were additionally separated by means of SFC. The structures were confirmed by their accurate masses and tandem mass spectrometry (MS/MS). A complementary quantification method was developed using SFC coupled to charged-aerosol detection (CAD) to overcome the disadvantages of quantification by means of MS without authentic standards. A flow compensation by varying the make-up flow was used to obtain a constant composition of the mobile phase during detection and to ensure a stable detector response. The concentrations of the individual liamocin species were determined using an external calibration with n-octyl-β-D-glycopyranoside. The total amount of these concentrations agrees with the dry weight of an aliquot of the heavy oil. The developed SFC-based method has the advantage of shorter analysis time and superior selectivity compared to the previously published LC separation. In brief, the here presented SFC hyphenations enable comprehensive analysis of liamocin biosurfactants providing identification and absolute quantification of individual congeners.
glycolipids, biosurfactants, high-resolution mass spectrometry, liamocins, charged-aerosol detection, supercritical fluid chromatography
Structure type: monomer ; 775.4450| New query | Export IDs | Home | Help |
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