Biosynthetic origin of benzoquinones in the explosive discharge of the bombardier beetleBrachinus elongatulus

被引:11
作者
Attygalle, Athula B. [1 ]
Xu, Sihang [1 ]
Moore, Wendy [2 ]
McManus, Reilly [2 ]
Gill, Aman [3 ]
Will, Kipling [3 ]
机构
[1] Stevens Inst Technol, Dept Chem & Chem Biol, Hoboken, NJ 07030 USA
[2] Univ Arizona, Dept Entomol, Tucson, AZ 85721 USA
[3] Univ Calif Berkeley, Dept Environm Sci Policy & Management, Berkeley, CA 94720 USA
来源
SCIENCE OF NATURE | 2020年 / 107卷 / 04期
基金
美国国家科学基金会;
关键词
Benzoquinone; Biosynthesis; Bombardier beetles; Brachinus elongatulus; Defensive secretions; DEFENSIVE SECRETION; COLEOPTERA CARABIDAE; ELEODES-LONGICOLLIS; BEETLES COLEOPTERA; CHEMICAL DEFENSES; ARTHROPODS; CHEMISTRY; QUINONE; GLANDS; SPRAY;
D O I
10.1007/s00114-020-01683-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bombardier beetles are well-known for their remarkable defensive mechanism. Their defensive apparatus consists of two compartments known as the reservoir and the reaction chamber. When challenged, muscles surrounding the reservoir contract sending chemical precursors into the reaction chamber where they mix with enzymes resulting in an explosive discharge of a hot noxious chemical spray containing two major quinones: 1,4-benzoquinone and 2-methyl-1,4-benzoquinone (toluquinone). Previously, it has been speculated that the biosynthesis of all benzoquinones originates from one core precursor, 1,4-hydroquinone. Careful ligation of the base of the reservoir chamber enabled us to prevent the explosive reaction and sample untransformed reservoir fluid, which showed that it accumulates significant quantities of 1,4-hydroquinone and 2-methyl-1,4-hydroquinone. We investigated the biosynthetic mechanisms leading to quinone formation by injecting or feedingBrachinus elongatulusbeetles with stable-isotope-labeled precursors. Chemical analysis of defensive secretion samples obtained from 1,4-hydroquinone-d(6)-administered beetles demonstrated that it underwent conversion specifically to 1,4-benzoquinone. Analogously, results fromm-cresol-d(8)injected or fed beetles confirmed thatm-cresol is metabolized to 2-methyl-1,4-hydroquinone, which is then oxidized to 2-methyl-1,4-benzoquinone in the hot spray. Our results refute the previous claim that 1,4-hydroquinone is the precursor of all substituted benzoquinones in bombardier beetles and reveal that they are biosynthetic products of two independent pathways. Most likely, the aforementioned biosynthetic channel of hydroxylation of appropriate phenolic precursors and subsequent oxidation is not restricted to bombardier beetles; it could well be a general pathway that leads to the formation of all congeners of benzoquinones, one of the most widely distributed groups of defensive compounds in arthropods.
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页数:11
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