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We describe a group of alloys that exhibit "super" properties, such as ultralow elastic modulus, ultrahigh strength, super elasticity, and super plasticity, at room temperature and that show Elinvar and Invar behavior. These "super" properties are attributable to a dislocation-free plastic deformation mechanism. In cold-worked alloys, this mechanism forms elastic strain fields of hierarchical structure that range in size from the nanometer scale to several tens of micrometers. The resultant elastic strain energy leads to a number of enhanced material properties.Mechanical properties, such as strength, of metallic materials are strongly affected by metallurgical processes such as heat treatment and plastic working, which bring modifications in the microstructure. On the other hand, these processes have no substantial effect on physical properties such as elastic modulus and thermal expansion. The reason for this is that the changes that can be affected by plastic working and heat treatment do not extend to interatomic bonds or electronic states.We present a group of alloys that exhibit multiple "super" properties and drastic changes in physical properties after plastic working at room temperature. These alloys simultaneously offer super elasticity, super strength, super coldworkability, and Invar and Elinvar properties. The alloys consist of Group IVa and Va elements and oxygen and share the following three electronic magic numbers: (i) a compositional average valence electron number [electron/atom (e/a) ratio] of about 4.24; (ii) a bond order (Bo value) of about 2.87 based on the DV-X␣ cluster method, which represents the bonding strength (1-3); and (iii) a "d" electron-orbital energy level (Md value) of about 2.45 eV, representing electronegativity. The properties emerge only when all three of these magic numbers are satisfied simultaneously. Various alloy composition combinations meet these criteria, such as Ti-12Ta-9Nb-3V-6Zr-O and Ti23Nb-0.7Ta-2Zr-O [mole percent (mol %)], wherein each alloy has a simple body-centered cubic (bcc) crystal structure. In order to exhibit these properties, each alloy system requires substantial cold working and the presence of a certain amount of oxygen, restricted to an oxygen concentration of 0.7 to 3.0 mol %.Typical properties of the alloys are shown in Fig. 1 for samples before and after cold swaging with 90% reduction in area (4). Tensile stress-strain curves shown in Fig. 1A indicate that cold working substantially decreases the elastic modulus and increases the yield strength and confirm nonlinearity in the elastic range, with the gradient of each curve decreasing continuously to about 1/3 its original value near the elastic limit. As a result of this decrease in elastic modulus and nonlinearity, elastic deformability after cold working reaches 2.5%, which is at least double the value before cold working. Generally, large elastic deformations that occur in so-called "super-elastic alloys" are known to be reversible martensitic transformations resulting from deformation, d...

A recombinant butanol pathway composed of Clostridium acetobutylicum ATCC 824 genes, thiL, hbd, crt, bcd-etfB-etfA, and adhe1 (or adhe) coding for acetyl-CoA acetyltransferase (THL), beta-hydroxybutyryl-CoA dehydrogenase (HBD), 3-hydroxybutyryl-CoA dehydratase (CRT), butyryl-CoA dehydrogenase (BCD), butyraldehyde dehydrogenase (BYDH), and butanol dehydrogenase (BDH), under the tac promoter control was constructed and was introduced into Escherichia coli. The functional expression of these six enzymes was proved by demonstrating the corresponding enzyme activities using spectrophotometric, high performance liquid chromatography and gas chromatography analyses. The BCD activity, which was not detected in E. coli previously, was shown in the present study by performing the procedure from cell extract preparation to activity measurement under anaerobic condition. Moreover, the etfA and etfB co-expression was found to be essential for the BCD activity. In the case of BYDH activity, the adhe gene product was shown to have higher specificity towards butyryl-CoA compared to the adhe1 product. Butanol production from glucose was achieved by the highly concentrated cells of the butanologenic E. coli strains, BUT1 with adhe1 and BUT2 with adhe, under anaerobic condition, and the BUT1 and BUT2 strains were shown to produce 4 and 16-mM butanol with 6- and 1-mM butyrate as a byproduct, respectively. This study reports the novel butanol production by an aerobically pregrown microorganism possessing the genes of a strict anaerobe, Clostridium acetobutylicum.

The Calvin cycle is the initial pathway of photosynthetic carbon fixation, and several of its reaction steps are suggested to exert rate-limiting influence on the growth of higher plants. Plastid fructose 1,6-bisphosphate aldolase (aldolase, EC 4.1.2.13) is one of the nonregulated enzymes comprising the Calvin cycle and is predicted to have the potential to control photosynthetic carbon flux through the cycle. In order to investigate the effect of overexpression of aldolase, this study generated transgenic tobacco (Nicotiana tabacum L. cv Xanthi) expressing Arabidopsis plastid aldolase. Resultant transgenic plants with 1.4-1.9-fold higher aldolase activities than those of wild-type plants showed enhanced growth, culminating in increased biomass, particularly under high CO₂ concentration (700 ppm) where the increase reached 2.2-fold relative to wild-type plants. This increase was associated with a 1.5-fold elevation of photosynthetic CO₂ fixation in the transgenic plants. The increased plastid aldolase resulted in a decrease in 3-phosphoglycerate and an increase in ribulose 1,5-bisphosphate and its immediate precursors in the Calvin cycle, but no significant changes in the activities of ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) or other major enzymes of carbon assimilation. Taken together, these results suggest that aldolase overexpression stimulates ribulose 1,5-bisphosphate regeneration and promotes CO₂ fixation. It was concluded that increased photosynthetic rate was responsible for enhanced growth and biomass yields of aldolase-overexpressing plants.