1986
DOI: 10.1021/np50047a005
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Biosynthesis of the Resistant Polymer in the Alga Botryococcus braunii. Studies on the Possible Direct Precursors

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Cited by 22 publications
(5 citation statements)
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“…These TAG may be difficult to extract due to their large molecular weight, though further analysis of intact TAG would be required to confirm this. Alternatively, B. braunii is known to produce degradation-resistant biopolymers that include the identified C28:1/C28:2 fatty acids [26], which may also explain this phenomenon.…”
Section: Discussionmentioning
confidence: 99%
“…These TAG may be difficult to extract due to their large molecular weight, though further analysis of intact TAG would be required to confirm this. Alternatively, B. braunii is known to produce degradation-resistant biopolymers that include the identified C28:1/C28:2 fatty acids [26], which may also explain this phenomenon.…”
Section: Discussionmentioning
confidence: 99%
“…COSY experiments established that in (73)- (75) the methine protons of the ether function resonated at 03.23 for H(10) and 3.43 for H(9'); the signal of proton H(lO'), on the hydroxyl-bearing carbon, appeared at 03.49 and the signal of proton H(9), attached to the ester-bearing carbon, was at 05.02. In structure (72), the protons were assigned on the basis of spectral comparisons with the diacetate derivative: protons H(9) and H(lO') on hydroxyl bearing carbons resonated at 03.57, whereas those attached to the carbons of the ether function, H (10) and H(9') were found at 03.32. The 13C-NMR spectra of (73)- (75) (72)- (74) and their TMS derivatives exhibited similar fragmentation modes giving ions of substantial diagnostic value, as shown in Fig.…”
Section: R -Ch -Ch-r /mentioning
confidence: 99%
“…Coupling might start by protonation of an epoxide (64), (65) or (66) followed by the specific cleavage of the C(9')-O bond; the carbocation formed would then attack a second epoxide (64) with concomitant cleavage of the C(9)-O bond. Then the positive charge at C(9) would be neutralized by reaction with water or a fatty acid, leading to (72) or (73)- (75), respectively.…”
Section: R -Ch -Ch-r /mentioning
confidence: 99%
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“…To test this hypothesis, we examined the effect of hydrophobic intracellular substances on hydrocarbon recovery efficiency from concentrated samples. Oleic acid, which is one of the main fatty acids in B. braunii race B , and a precursor of the biopolymer used to synthesize the colony matrix, , was used as a model hydrophobic intracellular compound. The concentrated sample filtered under the same conditions was used (dry cell weight ∼3 g/L).…”
Section: Resultsmentioning
confidence: 99%