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The Absolute Configurations of Hydroxy Fatty Acids from the Royal Jelly of Honeybees ( Apis mellifera )
Author(s) -
Kodai Tetsuya,
Nakatani Takafumi,
Noda Naoki
Publication year - 2011
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-010-3497-x
Subject(s) - royal jelly , queen (butterfly) , honey bee , absolute configuration , honey bees , worker bee , chemistry , metabolite , stereochemistry , biology , organic chemistry , biochemistry , botany , food science , hymenoptera
9‐Hydroxy‐2 E ‐decenoic acid (9‐HDA) is a precursor of the queen‐produced substance, 9‐oxo‐2 E ‐decenoic acid (9‐ODA), which has various important functions and roles for caste maintenance in honeybee colonies ( Apis mellifera ). 9‐HDA in royal jelly is considered to be a metabolite of 9‐ODA produced by worker bees, and it is fed back to the queen who then transforms it into 9‐ODA. Recently we found that 9‐HDA is present in royal jelly as a mixture of optical isomers ( R : S , 2:1). The finding leads us to suspect that chiral fatty acids in royal jelly are precursors of semiochemicals. Rather than looking for semiochemicals in the mandibular glands of the queen bee, this study involves the search for precursors of pheromones from large quantities of royal jelly. Seven chiral hydroxy fatty acids, 9,10‐dihydroxy‐2 E ‐decenoic, 4,10‐dihydroxy‐2 E ‐decenoic, 4 , 9‐dihydroxy‐2 E ‐decenoic, 3‐hydroxydecanoic, 3,9‐dihydroxydecanoic, 3,11‐dihydroxydodecanoic, and 3,10‐dihydroxydecanoic acids were isolated. The absolute configurations of these acids were determined using the modified Mosher's method, and it was revealed that, similar to 9‐HDA, five acids are present in royal jelly as mixtures of optical isomers.