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Featured researches published by David L. Hallahan.


Journal of Experimental Zoology | 2009

Analysis of Gene Expression in Gecko Digital Adhesive Pads Indicates Significant Production of Cysteine-and Glycine-Rich Beta-Keratins

David L. Hallahan; Natalie M. Keiper-Hrynko; Tanya Q. Shang; Thaya Silke Ganzke; Mattia Toni; Luisa Dalla Valle; Lorenzo Alibardi

Microscopic bristles (setae) present on digital pads permit the adhesion and climbing of geckos. Keratins of setae of the lizard Gekko gecko (Tokay gecko) were analyzed by the isolation of expressed mRNAs and by the generation of an EST library. Of the 510 sequences determined, 268 (52.9%) were unique. Of these, 14 appeared to encode alpha- and 111 beta-keratins. Within the beta-keratins, we identified five groups based on nucleotide sequence comparisons. Of these, one contained the bulk of beta-keratins, with 103 EST members. The mRNAs within this major group, together with two singlets, encoded cysteine-proline-serine-rich proteins of 10-14 kDa (Ge-cprp). One of the smaller groups of transcripts encoded slightly larger glycine-proline-serine-rich proteins, of 14-19 kDa (Ge-gprp). The remaining group consisted of smaller (9 kDa) serine-tyrosine-rich beta-keratins (Ge-strp). Thus three classes could be distinguished by amino acid sequence alignment. Exact matches for some of the peptide sequences obtained from setal proteins by ms/ms sequencing occur within several of these clones. Most of the beta-keratins were basic and contained a core-box region of two beta-strand sequences, with high homology to core-boxes present in avian scale and feather beta-keratins. Core-boxes are beta-folded regions that are likely responsible for polymerization into the beta-keratin filaments. The two deduced alpha-keratins of 52.7 kDa are both acidic, and contain the typical central rod region with some homology to mammalian and avian alpha-keratins, with variable N- and C-terminal regions. Basic beta-keratins and acidic alpha-keratins may interact electrostatically to form the resistant corneous material of setae.


Journal of Medical Entomology | 2008

Repellency of Hydrogenated Catmint Oil Formulations to Black Flies and Mosquitoes in the Field

Niketas C. Spero; Yamaira Gonzalez; Mark A. Scialdone; David L. Hallahan

Abstract The essential oil of catmint, Nepeta cataria L., was hydrogenated to yield an oil enriched in dihydronepetalactone (DHN) diastereomers, termed. This material was used for the preparation of liquid alcohol–based and lotion formulations. The efficacy of these formulations as repellents was tested after application to human test subjects at two locations in the United States: Maine and Florida. In Maine, data on repellency of the hydrogenated catmint oil formulations toward black flies (Simulium decorum Walker) and mosquitoes (primarily Aedes intrudens Dyar) were obtained. In these tests, protection from black flies was conferred for 6 h or more with all formulations, and both liquid and lotion formulations at 15 wt% active ingredient gave complete protection for 7.5 h. All formulations conferred protection from mosquitoes for >4 h, with the best (15 wt% lotion) giving >8 h of complete protection. In Florida, data on repellency toward a mixed population of mosquitoes indicated that all formulations conferred protection for >4 h, with the 15 wt% lotion giving >6 h complete protection from bites.


Journal of Medical Entomology | 2009

Dihydronepetalactones deter feeding activity by mosquitoes, stable flies, and deer ticks.

John E. Feaster; Mark A. Scialdone; Robin G. Todd; Yamaira Gonzalez; Joseph P. Foster; David L. Hallahan

ABSTRACT The essential oil of catmint, Nepeta cataria L., contains nepetalactones, that, on hydrogenation, yield the corresponding dihydronepetalactone (DHN) diastereomers. The DHN diastereomer (4R,4aR,7S,7aS)-4,7-dimethylhexahydrocyclopenta[c]pyran-l(3H)-one, DHN 1) was evaluated as mosquito repellent, as was the mixture of diastereomers {mostly (4S,4aR,7S,7aR)-4,7-dimethylhexahydrocyclopenta[c]pyran-1(3H)-one, DHN 2} present after hydrogenation of catmint oil itself. The repellency of these materials to Aedes aegypti L. and Anopheles albimanus Wiedemann mosquitoes was tested in vitro and found to be comparable to that obtained with the well-known insect repellent active ingredient N,N-diethyl-3-methylbenzamide (DEET). DHN 1 and DHN 2 also repelled the stable fly, Stomoxys calcitrans L., in this study. DHN 1, DHN 2, and p-menthane-3,8-diol (PMD), another natural monoterpenoid repellent, gave comparable levels of repellency against An. albimanus and S. calcitrans. Laboratory testing of DHN 1 and DHN 2 using human subjects with An. albimanus mosquitoes was carried out. Both DHN 1 and DHN 2 at 10% (wt:vol) conferred complete protection from bites for significant periods of time (3.5 and 5 h, respectively), with DHN2 conferring protection statistically equivalent to DEET. The DHN 1 and DHN 2 diastereomers were also efficaceous against black-legged tick (Ixodes scapularis Say) nymphs.


Archive | 2003

Insect repellent compositions comprising dihydronepetalactone

David L. Hallahan; Leo Ernest Manzer


Archive | 2003

Dihydronepetalactone as insect repellent

David L. Hallahan


Archive | 2003

Cis-prenyltransferases from the rubber-producing plants russian dandelion (taraxacum kok-saghyz) and sunflower (helianthus annus)

David L. Hallahan; Natalie M. Keiper-Hrynko


Archive | 2004

Method for manipulating growth, yield, and architecture in plants

David L. Hallahan; Natalie M. Keiper-Hrynko


Archive | 2002

Polynucleotides encoding an acetyl-CoA acetyltransferase from Hevea brasiliensis, related products, and methods

David L. Hallahan; Natalie M. Keiper-Hrynko


Archive | 2012

PLANT ARTIFICIAL SEEDS HAVING MULTILAYERS AND METHODS FOR THE PRODUCTION THEREOF

Timothy Caspar; Denise Gaspareto; Lawrence Doka Gaultney; Ross Gilmour; Beverly Hallahan; David L. Hallahan; Barry D. Johnson; Brad H. Jones; Katrina Kratz; Prakash Lakshmanan; Surbhi Mahajan; Brian D. Mather; Barry Alan Morris; Marcos Luciano Nunhez; Joseph Anthony Perrotto; Jingjing Xu


Archive | 2009

Method for making insect repellent composition

David L. Hallahan; Leo Ernest Manzer

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