TY - JOUR
T1 - Salicylhydroxamic acid inhibits Δ6 desaturation in the microalga Porphyridium cruentum
AU - Khozin-Goldberg, Inna
AU - Bigogno, Chiara
AU - Cohen, Zvi
N1 - Funding Information:
We are grateful to Ms. S. Didi for dedicated technical assistance. This research was supported in part by the Israeli Ministry of Art and Sciences. I.K. is the recipient of a Gileadi fellowship from the Israeli Ministry of Absorption.
PY - 1999/8/18
Y1 - 1999/8/18
N2 - Treatment of the microalga Porphyridium cruentum with salicylhydroxamic acid (SHAM) inhibited growth and affected fatty acid composition. At a relatively low concentration (40 μM) SHAM predominantly inhibits Δ6 desaturation. The effect of the inhibitor was most intense in phosphatidylcholine (PC) and phosphatidylethanolamine, in which the proportions of the downstream products of the Δ6 desaturase were reduced, whereas that of the substrate, 18:2, increased. As a result of the availability of 18:2, 18:3ω3, which under normal conditions is not observed, appeared predominantly in chloroplastic lipids. Pulse labeling with linoleic acid has shown that SHAM inhibits Δ6 desaturation almost immediately, suggesting an apparent inhibition of the activity of the desaturase, rather than its synthesis or that of its cofactors. Furthermore, the addition of γ-linolenic acid to SHAM-inhibited cultures relieved the inhibition. Following exposure to the inhibitor, 18:3ω3 appeared first in chloroplastic glycolipids and only later in PC, indicating that the former are the substrates for the first dedicated step of the proposed ω3 pathway in this alga. Copyright (C) 1999 Elsevier Science B.V.
AB - Treatment of the microalga Porphyridium cruentum with salicylhydroxamic acid (SHAM) inhibited growth and affected fatty acid composition. At a relatively low concentration (40 μM) SHAM predominantly inhibits Δ6 desaturation. The effect of the inhibitor was most intense in phosphatidylcholine (PC) and phosphatidylethanolamine, in which the proportions of the downstream products of the Δ6 desaturase were reduced, whereas that of the substrate, 18:2, increased. As a result of the availability of 18:2, 18:3ω3, which under normal conditions is not observed, appeared predominantly in chloroplastic lipids. Pulse labeling with linoleic acid has shown that SHAM inhibits Δ6 desaturation almost immediately, suggesting an apparent inhibition of the activity of the desaturase, rather than its synthesis or that of its cofactors. Furthermore, the addition of γ-linolenic acid to SHAM-inhibited cultures relieved the inhibition. Following exposure to the inhibitor, 18:3ω3 appeared first in chloroplastic glycolipids and only later in PC, indicating that the former are the substrates for the first dedicated step of the proposed ω3 pathway in this alga. Copyright (C) 1999 Elsevier Science B.V.
KW - Biosynthesis
KW - Eicosapentaenoic acid
KW - Fatty acid desaturation
KW - Microalga
KW - Porphyridium
KW - Salicylhydroxamic acid
UR - http://www.scopus.com/inward/record.url?scp=0032779439&partnerID=8YFLogxK
U2 - 10.1016/S1388-1981(99)00107-9
DO - 10.1016/S1388-1981(99)00107-9
M3 - Article
AN - SCOPUS:0032779439
SN - 1388-1981
VL - 1439
SP - 384
EP - 394
JO - Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
JF - Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
IS - 3
ER -