Science 2012-11-09

A core metabolic enzyme mediates resistance to phosphine gas.

David I Schlipalius, Nicholas Valmas, Andrew G Tuck, Rajeswaran Jagadeesan, Li Ma, Ramandeep Kaur, Anita Goldinger, Cameron Anderson, Jujiao Kuang, Steven Zuryn, Yosep S Mau, Qiang Cheng, Patrick J Collins, Manoj K Nayak, Horst Joachim Schirra, Massimo A Hilliard, Paul R Ebert

Index: Science 338(6108) , 807-10, (2012)

Full Text: HTML

Abstract

Phosphine is a small redox-active gas that is used to protect global grain reserves, which are threatened by the emergence of phosphine resistance in pest insects. We find that polymorphisms responsible for genetic resistance cluster around the redox-active catalytic disulfide or the dimerization interface of dihydrolipoamide dehydrogenase (DLD) in insects (Rhyzopertha dominica and Tribolium castaneum) and nematodes (Caenorhabditis elegans). DLD is a core metabolic enzyme representing a new class of resistance factor for a redox-active metabolic toxin. It participates in four key steps of core metabolism, and metabolite profiles indicate that phosphine exposure in mutant and wild-type animals affects these steps differently. Mutation of DLD in C. elegans increases arsenite sensitivity. This specific vulnerability may be exploited to control phosphine-resistant insects and safeguard food security.


Related Compounds

Related Articles:

Suppressor of Deltex mediates Pez degradation and modulates Drosophila midgut homeostasis.

2015-01-01

[Nat. Commun. 6 , 6607, (2015)]

Molybdenum complex with bulky chelates as a functional model for molybdenum oxidases.

2014-12-01

[Inorg. Chem. 53(23) , 12416-27, (2014)]

Experimental and theoretical mechanistic investigation of the iridium-catalyzed dehydrogenative decarbonylation of primary alcohols.

2015-01-21

[J. Am. Chem. Soc. 137(2) , 834-42, (2015)]

Surface functionalisation of carbon for low cost fabrication of highly stable electrochemical DNA sensors.

2015-09-15

[Biosens. Bioelectron. 71 , 25-9, (2015)]

LDL-R promoting activity of peptides derived from human PCSK9 catalytic domain (153-421): design, synthesis and biochemical evaluation.

2015-03-06

[Eur. J. Med. Chem. 92 , 890-907, (2015)]

More Articles...