Activity of two lignin biosynthesis enzymes during development of a maize internode

To ascertain the temporal relationships of phcnylpropanoid and lignin pathway enzymes, phenylalanine ammonia-lyase (PAL) and cinnamyl alcohol- NADPH dehydrogenase(CAD), with lignin concentration, PAL and CAD activities and lignin concentrations were assessed during progressive development of the 10th internode in maize (Zea mays L). Enzyme activities were quantified and lignin concentrations were determined by the detergent system of fiber fractiona- tion from lower, middle, and upper sections of the elongating internode harvested 3, 5, 7, 9, 11, 13, and 15 days after the internode had reached 10 mm in length. Over 15 days, a coordinated, sequential, and basipetal pattern of enzyme activities and lignin accumulation evolved through the internode, spanning the stages of rapid elongation, cellular differentiation, and secondary cell wall formation. PAL activity was initiated first, rising to peak activity in elongating tissue, and falling basipetally in tissues as they matured. CAD activity rose in fully elongated, maturing internode tissue where PAL activity was waning following its peak activity. Lignin accumulated in tissues with high CAD activity. CAD activity and lignin deposition patterns were similar: simultaneously increasing in activity and deposition over time while activity and deposition also shifting basipetally through the internode, keeping pace with secondary cell wall formation. Lignin concentration correlated significantly with CAD, but not with PAL.     

A novel technique for the preparation of secondary fatty amides

A technique for the synthesis of monosubstituted fatty amides at low temperature and ambient pressure was developed. This method involved the condensation of an amine with a triacylglycerol. The primary amine (ethyl,n-butyl,n-hexyl andn-octyl were tested) acted as reagent and solvent for the fatty substrates. No additional organic solvent or catalyst was added. Tallow, vegetable oils and fish oil all served well as substrates, as did pure tripalmitin. The rate of amidation was dependent upon temperature and the ratio of fat to amine. In a series of experiments conducted with tallow andn-butylamine at a fat:amine molar ratio of 1:16, amidation could be carried out at 20°C, producingn-butyltallowamide in 83% yield in 24 hr. When the fat:amine molar ratio was reduced to 1:8, and the temperature raised to 45°C, the amide yield was 87.6% in 24 hr. When the reaction was carried out at the boiling point ofn-butylamine (78°C) and at a fat:amine ratio of 1:8, the amide yield was 93.2% in 4 hr. The reaction progressed more rapidly with higher molecular weight amines. The identity and purity of the amides was assessed by thin-layer chromatography and confirmed by elemental analyses and infrared and C¹³ nuclear magnetic resonance spectroscopy.     

Synthesis, Sintering, Microstructure, and Mechanical Properties of Ceramics Made by Exothermic Reactions

Al₂O₃-TiC, Al₂O₃-TiC_0.5N_0.5, Al₂O₃-WC, Al₂O₃-SiC, and Al₂O₃-HfB₂ powders were synthesized by the aluminothermic reduction of oxides in the presence of carbon or boron. The reacted powders were milled to reduce the size of agglomerates and subsequently densified without applied pressure to near-theoretical density. Microstructures and mechanical properties of composites made from exothermically reacted powders were compared with similar ceramics made from commercially available powders. In situ sintering was possible in the Al₂O₃-TiC system using a closed graphite crucible to contain reaction gases. The synthesis of β -SiC at temperatures above 1400°C via the direct reaction of the elements (SHS) was compared with SiC made by the magnesiothermic reduction of SiO₂ in the presence of C after removing the MgO by leaching.     

Nonlinear decoupling control in the presence of sensor and actuator deadtimes

This work focuses on synthesizing nonlinear decoupling controllers for multivariable nonlinear systems represented by a state-space model, in the presence of deadtimes. The deadtimes appear in both the inputs and the outputs, but not in the states, and are physically associated with sensors and actuators. Simple sufficient conditions for feasibility of closed-loop deadtimes are derived, which rely only on the structural properties of the system. A control law is then derived so that the closed-loop system is input/output linear and decoupled, with deadtimes equal to the smallest ones that satisfy the feasibility conditions. The proposed method is applied to a chemical process. Its performance is evaluated through simulation in the presence of set-point and disturbance changes.     

A Fragrance Prediction Model for Molecules Using Rough Set-based Machine Learning

In this work, a novel machine learning based methodology was developed to predict fragrance from the molecular structure and the effect of the subjects attributes on odour perception. As fragrance is linked to the molecular structure and interactions, topological indices are used to develop a predictive model. Rough set-based machine learning is used to generate rule-based models that link the topology of fragrant molecules and dilution to their respective odour characteristics. The results show that the generated models are effective in determining the odour characteristic of molecules.     

Competing Effects of Radio Frequency Fields on Carbon Nanotube/Resin Systems: Alignment versus Heating

This work shows that radio-frequency (RF) fields can simultaneously align carbon nanotubes (CNTs) dispersed in a resin and induce Joule heating to cure the resin. The timescales of alignment and curing using RF heating are numerically computed and compared at different field strengths in order to determine a temperature where alignment happens before the matrix crosslinks. Composites are experimentally fabricated at the desired target temperature and are optically analyzed and quantified; the CNT network is successfully aligned in the direction of the applied electric field. This methodology can be used to create composites where the local alignment can be varied across the sample. Composites fabricated using RF fields have higher electrical conductivity in the direction of the aligned CNTs than an oven-cured, randomly aligned sample. Also, RF-cured nanocomposites exhibit higher tensile strength and modulus in the direction of alignment compared to an oven-cured sample. Finally, it is further demonstrated how this methodology can be coupled with a direct ink writing additive manufacturing process to induce alignment in any desired direction, even orthogonal to the shear forces in the extrusion direction.     

Chromophore‐Linked Substrate (CLS405): Probing Metallo‐β‐Lactamase Activity and Inhibition

Serine‐ and metallo‐β‐lactamases present a threat to the clinical use of nearly all β‐lactam antibiotics, including penicillins, cephalosporins, and carbapenems. Efforts to develop metallo‐β‐lactamase (MBL) inhibitors require suitable screening platforms to allow the rapid determination of β‐lactamase activity and efficient inhibition. Unfortunately, the platforms currently available are not ideal for this purpose. Further progress in MBL inhibitor identification requires inexpensive and widely applicable assays. Herein the identification of an inexpensive and stable chromogenic substrate suitable for use in assays of clinically relevant MBLs is described. (6R,7R)‐3‐((4‐Nitrophenoxy)methyl)‐8‐oxo‐7‐(2‐phenylacetamido)‐5‐thia‐1‐azabicyclo[4.2.0]oct‐2‐ene‐2‐carboxylic acid 5,5‐dioxide (CLS405) was synthesised in a three‐step protocol. CLS405 was then characterised spectroscopically, and its stability and kinetic properties evaluated. With a Δλ_max value of 100 nm between the parent and hydrolysis product, a higher analytical accuracy is possible with CLS405 than with commonly used chromogenic substrates. The use of CLS405 in assays was validated by MBL activity measurements and inhibitor screening that resulted in the identification of N‐hydroxythiazoles as new inhibitor scaffolds for MBLs. Further evaluation of the identified N‐hydroxythiazoles against a panel of clinically relevant MBLs showed that they possess inhibitory activities in the mid‐ to low‐micromolar range. The findings of this study provide both a useful tool compound for further inhibitor identification, and novel scaffolds for the design of improved MBL inhibitors with potential as antibiotics against resistant strains of bacteria.     

Planning of carbon capture and storage with pinch analysis techniques

Carbon capture and storage (CCS) is a means for reducing carbon dioxide (CO₂) emissions from fossil fuel combustion in power generation and industrial processes. It involves the capture of CO₂ for subsequent storage in various geological formations. The selection and matching of the power plants and storage sites are often an issue of optimisation due to various constraints, i.e., time of availability, injection rate, and storage capacity limits. In this work, a novel graphical targeting tool based on pinch analysis is proposed to address the planning problem of the storage of captured CO₂ from power generating plants into corresponding reservoirs. The main consideration for the problem is the time of availability of the latter, since reservoirs need to be developed prior to CO₂ storage. The time limitation is addressed by the graphical technique where time is taken as the governing element in solving the problem. Hypothetical examples are used to elucidate the proposed approach.     

Progress in Block Copolymers

Monodisperse proteins and polydisperse carbohydrates and polyenes occur in nature. The proteins are random copolymers, but no block or graft copolymers occur in nature.     

The stability of direct carbon fuel cells with molten Sb and Sb–Bi alloy anodes

The long‐term stability of direct carbon fuel cells, based on solid oxide fuel cells with molten Sb and Sb–Bi anodes, was examined for operation with activated charcoal, rice starch, and bio‐oil fuels at 973 K. With intermittent stirring of the fuel–metal anode interface, the anode performance was stable, and reasonable power densities (～250 mW/cm²) were achieved for periods up to 250 h. With Sc‐stabilized zirconia, severe thinning of the electrolyte occurred in regions of high current flow. No electrolyte thinning was observed with yttria‐stabilized zirconia as the electrolyte operating at the same current densities. © 2012 American Institute of Chemical Engineers AIChE J, 59: 3342–3348, 2013