Herbivore Gender Effects on Volatile Induction in Aspen and on Olfactory Responses in Leaf Beetles

Hybrid aspen (Populus tremula × tremuloides Michx.) is a fast-growing tree species used for short-rotation forestry in northern latitudes. Aspen species have a rich herbivore fauna, including defoliating leaf beetles that induce emissions of volatile organic compounds (VOCs) when feeding on aspen leaves. We investigated the differential induction of VOCs by male and female Phratora laticollis leaf beetles feeding on hybrid aspen and the differences in the orientation of beetles in response to gender-specific induced VOCs. The hypotheses for the study were (1) the VOCs in the headspace of plants infested with beetles of the two genders individually and in mixed aggregates would vary subtly, and (2) foraging adult beetles would be able to detect differences in VOC blends and use them to fine-tune their orientation choices. In Y-tube bioassays, both females and males preferred VOCs from leaves damaged by one gender (females or males) over undamaged leaves. However, if leaves were damaged by a two-gender population, neither females nor males indicated a preference over volatiles of undamaged leaves. Leaves damaged by both beetle genders simultaneously had significantly increased green leaf volatile (GLV), benzenoid and homoterpene emissions compared to undamaged leaves. Emissions of these compounds possibly indicate higher herbivore pressure and a higher risk of attack by parasitoids and predators and could thus be the cause of the lack of beetle preference. Our findings provide new basic information on gender-based host plant selection by herbivores and may be helpful in the development of sustainable biogenic VOC-based herbivore-control methods for intensive short-rotation hybrid aspen production

Roles of the A and C Sites in the Manganese-Specific Activation of MntR

The manganese transport regulator (MntR) represses the expression of genes involved in manganese uptake in <i>Bacillus subtilis</i>. It selectively responds to Mn²⁺ and Cd²⁺ over other divalent metal cations, including Fe²⁺, Co²⁺, and Zn²⁺. Previous work has shown that MntR forms binuclear complexes with Mn²⁺ or Cd²⁺ at two binding sites, labeled A and C, that are separated by 4.4 Å. Zinc activates MntR poorly and binds only to the A site, forming a mononuclear complex. The difference in metal binding stoichiometry suggested a mechanism for selectivity in MntR. Larger metal cations are strongly activating because they can form the binuclear complex, while smaller metal ions cannot bind with the geometry needed to fully occupy both metal binding sites. To investigate this hypothesis, structures of MntR in complex with two other noncognate metal ions, Fe²⁺ and Co²⁺, have been determined. Each metal forms a mononuclear complex with MntR with the metal ion bound in the A site, supporting the conclusions drawn from the Zn²⁺ complex. Additionally, we investigated two site-specific mutants of MntR, E11K and H77A, that contain substitutions of metal binding residues in the A site. While metal binding in each mutant is significantly altered relative to that of wild-type MntR, both mutants retain activity and selectivity for Mn²⁺ in vitro and in vivo. That observation, coupled with previous studies, suggests that the A and C sites both contribute to the selectivity of MntR