No abstract

Recombinant polyesterase (Est119) from Thermobifida alba AHK119 was purified by two chromatography steps. The final protein was observed as a single band in SDS-PAGE, and the specific activity of Est119 for p-nitrophenyl butyrate was 2.30 u/mg. Purified Est119 was active with aliphatic and aliphatic-co-aromatic polyesters. Kinetic data indicated that p-nitrophenyl butyrate (pNPB) or hexanoate was the best substrate for Est119 among p-nitrophenyl acyl esters. Calcium was required for full activity and thermostability of Est119, which was stable at 50 °C for 16 h. Three-dimensional modeling and biochemical characterization showed that Est119 is a typical cutinase-type enzyme that has the compact ternary structure of an α/β-hydrolase. Random and site-directed mutagenesis of wild-type Est119 resulted in improved activity with increased hydrophobic interaction between the antiparallel first and second β-sheets (A68V had the greatest effect). Introduction of a proline residue (S219P) in a predicted substrate-docking loop increased the thermostability. The specific activity of the A68V/S219P mutant on pNPB was increased by more than 50-fold over the wild type. The mutant was further activated by 2.6-fold (299 u/mg) with 300 mM Ca(2+) and was stable up to 60 °C with 150 mM Ca(2+). Another identical gene was located in tandem in the upstream of est119.

No abstract

Precision frequency measurements of terahertz (THz) waves are required to establish metrology in the THz spectral region. However, frequency measurement techniques in this region are immature. We propose a THz spectrum analyzer to measure the absolute frequency and spectral shape of continuous-wave THz waves. Based on a stable frequency comb generated in a photoconductive antenna, the absolute frequency of a sub- THz test source was determined at a precision of 2.8 x 10(-11). Furthermore, the spectral bandwidth of the THz spectrum analyzer can be extended over 1 THz, as demonstrated by measurement of a THz test source. This spectrum analyzer has the potential to become a powerful tool for THz frequency metrology.

To enhance the Chromobacterium viscosum lipase (glycerol-ester hydrolase; EC 3.1.1.3) activity for the reaction of water-insoluble substrates, the AOT/isooctane reverse micellar interface was modi®ed by co-adsorption of a non-ionic surfactant. Polyoxyethylene sorbitan trioleate (Tween 85) was used as the non-ionic surfactant and olive oil as a water-insoluble substrate. An appreciable increase of lipase activity was observed and at higher W o values (where W o = molar ratio of water to total surfactants of the micellar system) there was no sharp fall of the enzyme activity such as a typical bell-shaped pro®le. The kinetic model for the lipase-catalysed hydrolysis of olive oil in AOT/isooctane reverse micellar system was applied to the enzymatic reaction in this mixed reverse micellar system. It was found that the predictions of the model agree well with the experimental kinetic results and that the adsorption equilibrium constant of olive oil molecules between the micellar phase and the bulk phase of the organic solvent is smaller in AOT/Tween 85 mixed reverse micellar systems than in simple AOT reverse micellar systems.