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Andrew C Miller

Publications and source records attributed to Andrew C Miller.

5 recordsLinked to original sources
PubMed2006

Creating patterned carbon nanotube catalysts through the microcontact printing of block copolymer micellar thin films.

We report a route for synthesizing patterned carbon nanotube (CNT) catalysts through the microcontact printing of iron-loaded poly(styrene-block-acrylic acid) (PS-b-PAA) micellar solutions onto silicon wafers coated with thin aluminum oxide (Al(2)O(3)) layers. The amphiphilic block copolymer, PS-b-PAA, forms spherical micelles in toluene that can form quasi-hexagonal arrays of spherical PAA domains within a PS matrix when deposited onto a substrate. In this report, we dip a poly(dimethylsiloxane) (PDMS) molded stamp into an iron-loaded micellar solution to create a thin film on the PDMS features. The PDMS stamp is then put in contact with a substrate, and uniaxial compressive stress is applied to transfer the micellar thin film from the PDMS stamp onto the substrate in a defined pattern. The polymer is then removed by oxygen plasma etching to leave a patterned iron oxide nanocluster array on the substrate. Using these catalysts, we achieve patterned vertical growth of multiwalled CNTs, where the CNTs maintain the fidelity of the patterned catalyst, forming high-aspect-ratio standing structures.

Acrylates↗
PubMed2004

Reducing risks of maintenance dredging on freshwater mussels (Unionidae) in the Big Sunflower River, Mississippi.

In response to proposed dredging in a 122-km reach of the Big Sunflower River, Mississippi, we studied freshwater mussels (family: Unionidae) using qualitative, semi-quantitative, and quantitative (0.25 m(2) total substratum removal) methods in 1987, 1993, 1994, 2001, 2002, and 2003. Our objectives were to identify important mussel resources, to devise methods for minimizing dredging risks, and to identify habitat improvement features. Approximately 60% of the fauna was located on two high-density shoals characterized by extreme dominance of the commercially valuable threeridge (Amblema plicata). Shallow nearshore and main channel areas comprised approximately 10 and 88% of the aquatic habitat in the project area; however, these areas were of less importance for mussels and supported densities of approximately 5 and 0.5 individuals/m(2), respectively. Throughout the project area the mussel fauna exhibited little or no evidence of recent recruitment, dominance of relatively few species (either A. plicata, or the bank climber Plectomerus dombeyanus), and low species diversity (H') and evenness. No federally listed endangered or threatened mussels were found, although the pyramid pigtoe (Pleurobema pyramidatum), a species listed as endangered in Mississippi, was collected in and upstream of the project area. Two other state-listed species, Plethobasus cyphyus (sheepnose) and Quadrula cylindrica (rabbitsfoot), were only found on gravelly shoals upriver of the project area. Maintenance plans were redesigned to minimize environmental damage; a hydraulic cutterhead dredge will be used in most of the mainstem to reduce risk to nearshore habitats. High-density assemblages on four shoals will not be dredged and 150 and 100 m buffer zones will be left immediately up and downriver. Enhancements for aquatic biota will be created with gravel substratum and wing dams.

Animals↗
PubMed2004

Methylation-independent aerotaxis mediated by the Escherichia coli Aer protein.

Aer is a membrane-associated protein that mediates aerotactic responses in Escherichia coli. Its C-terminal half closely resembles the signaling domains of methyl-accepting chemotaxis proteins (MCPs), which undergo reversible methylation at specific glutamic acid residues to adapt their signaling outputs to homogeneous chemical environments. MCP-mediated behaviors are dependent on two specific enzymes, CheR (methyltransferase) and CheB (methylesterase). The Aer signaling domain contains unorthodox methylation sites that do not conform to the consensus motif for CheR or CheB substrates, suggesting that Aer, unlike conventional MCPs, might be a methylation-independent transducer. Several lines of evidence supported this possibility. (i) The Aer protein was not detectably modified by either CheR or CheB. (ii) Amino acid replacements at the putative Aer methylation sites generally had no deleterious effect on Aer function. (iii) Aer promoted aerotactic migrations on semisolid media in strains that lacked all four of the E. coli MCPs. CheR and CheB function had no influence on the rate of aerotactic movements in those strains. Thus, Aer senses and signals efficiently in the absence of deamidation or methylation, methylation changes, methylation enzymes, and methyl-accepting chemotaxis proteins. We also found that chimeric transducers containing the PAS-HAMP sensing domain of Aer joined to the signaling domain and methylation sites of Tar, an orthodox MCP, exhibited both methylation-dependent and methylation-independent aerotactic behavior. The hybrid Aear transducers demonstrate that methylation independence does not emanate from the Aer signaling domain but rather may be due to transience of the cellular redox changes that are thought to trigger Aer-mediated behavioral responses.

Amino Acid Sequence↗