A Model of Enzymatic Nitrite Reduction in Corn (Zea Mays L.)

152 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1975.U of I OnlyRestricted to the U of I community idenfinitely during batch ingest of legacy ETD

Nitrate Assimilation Limits Nitrogen Use Efficiency (NUE) in Maize (Zea mays L.)

Grain yield in maize responds to N fertility in a linear-plateau fashion with nitrogen use efficiency (NUE) higher under lower N fertilities and less as grain yield plateaus. Field experiments were used to identify plant parameters relative for improved NUE in maize and then experiments were performed under controlled conditions to elucidate metabolism controlling these parameters. Field experiments showed reproductive parameters, including R1 ear-weight, predictive of N response under both high and low NUE conditions. R1 ear-weight could be changed by varying nitrate concentrations early during reproductive development but from V12 onward R1 ear-weight could be changed little by increasing or decreasing nitrate fertility. Ammonia, on the other hand, could rescue R1 ear-weight as late as V15 suggesting nitrate assimilation (NA) limits ear development response to N fertility since bypassing NA can rescue R1 ear-weight. Nitrate reductase activity (NRA (in vitro)) increases linearly with nitrate fertility but in vivo nitrate reductase activity (NRA (in vivo)) follows organic N accumulation, peaking at sufficient levels of nitrate fertility. The bulk of the increase in total plant N at high levels of nitrate fertility is due to increased plant nitrate concentration. Increasing NADH levels by selective co-suppression of ubiquinone oxidoreductase 51 kDa subunit (Complex I) was associated with improved grain yield by increasing ear size, as judged by increased kernel number plant−1 (KNP), and increased NRA (in vivo) without a change in NRA (in vitro). These results support NUE is limited in maize by NA but not by nitrate uptake or NRA (in vitro)

Electrochemical Properties of Metal-Oxide-Coated Carbon Electrodes Prepared by Atomic Layer Deposition

Here we report on the electrochemical properties of carbon electrodes coated with thin layers of Al₂O₃ and SnO₂. These oxide films were deposited using atomic layer deposition (ALD) and range in thickness from 1 to 6 nm. Electrochemical experiments show that the thinnest oxide layers contain defects that penetrate to the underlying carbon electrode. However, oxygenation of the carbon surface prior to ALD increases the surface concentration of nucleation sites for oxide growth and suppresses the defect density. Films of Al₂O₃ just ∼3–4 nm in thickness are free of pinholes. Slightly thicker coatings of SnO₂ are required for equivalent passivation. Both Al₂O₃ and SnO₂ films are stable in both neutral and acidic electrolytes even after repeated voltammetric scanning. The results reported here open up the possibility of studying the effect of oxide supports on electrocatalytic reactions

Multistep Galvanic Exchange Synthesis Yielding Fully Reduced Pt Dendrimer-Encapsulated Nanoparticles

Here we outline a new method for synthesizing fully reduced Pt dendrimer-encapsulated nanoparticles (DENs). This is achieved by first synthesizing Cu DENs of the appropriate size through sequential dendrimer loading and reduction steps, and then galvanically exchanging the zerovalent Cu DENs for Pt. The properties of Pt DENs having an average of 55, 140, and 225 atoms prepared by direct chemical reduction and by galvanic exchange are compared. Data obtained by UV–vis spectroscopy, X-ray absorption spectroscopy, X-ray photoelectron spectroscopy, and high-resolution electron microscopy confirm only the presence of fully reduced Pt DENs when synthesized by galvanic exchange, while chemical reduction leads to a mixture of reduced DENs and unreduced precursor. These results are significant because Pt DENs are good models for developing a better understanding of the effects of finite size on catalytic reactions. Until now, however, the results of such studies have been complicated by a heterogeneous mixture of Pt catalysts