New C40-carotenoid acyl glycoside as principal carotenoid in Salinibacter ruber, an extremely halophilic eubacterium

Bjart Frode Lutnaes; Aharon Oren; Synnøve Liaaen-Jensen

doi:10.1021/np020125c

New C₄₀-carotenoid acyl glycoside as principal carotenoid in Salinibacter ruber, an extremely halophilic eubacterium

Bjart Frode Lutnaes
, Aharon Oren
, Synnøve Liaaen-Jensen^*

^*Corresponding author for this work

Alexander Silberman Institute of Life Sciences

Research output: Contribution to journal › Article › peer-review

81 Scopus citations

Abstract

The principal (>96% of total) carotenoid in the novel, extremely halophilic eubacterium Salinibacter ruber, here called salinixanthin (1), has been assigned the structure (all-E,2′S)-2′-hydroxy-1′-[6-O-(13-methyltetradecanoyl) -β-D-glycopyranosyloxy]-3′,4′-didehydro-1′, 2′-dihydro-β,ψ-caroten-4-one by spectrometric (vis, EIMS, ¹HNMR, CD, GCMS) and chemical methods.

Original language	English
Pages (from-to)	1340-1343
Number of pages	4
Journal	Journal of Natural Products
Volume	65
Issue number	9
DOIs	https://doi.org/10.1021/np020125c
State	Published - 1 Sep 2002

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title = "New C40-carotenoid acyl glycoside as principal carotenoid in Salinibacter ruber, an extremely halophilic eubacterium",

abstract = "The principal (>96\% of total) carotenoid in the novel, extremely halophilic eubacterium Salinibacter ruber, here called salinixanthin (1), has been assigned the structure (all-E,2′S)-2′-hydroxy-1′-[6-O-(13-methyltetradecanoyl) -β-D-glycopyranosyloxy]-3′,4′-didehydro-1′, 2′-dihydro-β,ψ-caroten-4-one by spectrometric (vis, EIMS, 1HNMR, CD, GCMS) and chemical methods.",

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AU - Lutnaes, Bjart Frode

AU - Oren, Aharon

AU - Liaaen-Jensen, Synnøve

PY - 2002/9/1

Y1 - 2002/9/1

N2 - The principal (>96% of total) carotenoid in the novel, extremely halophilic eubacterium Salinibacter ruber, here called salinixanthin (1), has been assigned the structure (all-E,2′S)-2′-hydroxy-1′-[6-O-(13-methyltetradecanoyl) -β-D-glycopyranosyloxy]-3′,4′-didehydro-1′, 2′-dihydro-β,ψ-caroten-4-one by spectrometric (vis, EIMS, 1HNMR, CD, GCMS) and chemical methods.

AB - The principal (>96% of total) carotenoid in the novel, extremely halophilic eubacterium Salinibacter ruber, here called salinixanthin (1), has been assigned the structure (all-E,2′S)-2′-hydroxy-1′-[6-O-(13-methyltetradecanoyl) -β-D-glycopyranosyloxy]-3′,4′-didehydro-1′, 2′-dihydro-β,ψ-caroten-4-one by spectrometric (vis, EIMS, 1HNMR, CD, GCMS) and chemical methods.

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JO - Journal of Natural Products

JF - Journal of Natural Products

IS - 9

ER -

New C₄₀-carotenoid acyl glycoside as principal carotenoid in Salinibacter ruber, an extremely halophilic eubacterium

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