Modulation transfer spectroscopy of coherent population trapping based on phase-coherent lasers.

A new source of two diode laser beams, spatially separated but optically phase-locked with each other, is used to study the modulation transfer spectroscopy of coherent population trapping resonance (CPT). The spectrum for the (87)Rb D2 line is obtained with narrow linewidth and high signal-to-noise ratio, and analyzed with different experimental parameters. A theoretical analysis of the CPT modulation transfer spectra is deduced from the density matrix equation of motion, and found to be in good agreement with the experimental results.

Study of phase coherence degradation induced by a tapered semiconductor amplifier with frequency-modulated continuous-wave and pulsed seed lasers.

We investigate the phase coherence between a seed laser and a laser amplified by a tapered semiconductor amplifier (TSA) when the seed laser is either continuous wave (CW) or pulsed. The phase fluctuations in the time domain are employed to describe the degradation of phase coherence induced by a TSA. The amplified laser is measured to be approximately 99.98% coherent with the seed, when the CW or pulsed laser is seeded, at different supplying currents of the TSA. Furthermore, the phase coherence is measured when the seed laser is modulated. The results reveal that the phase coherence degradations induced by the TSA remain the same for a seed laser with and without modulation, when different supplying currents of the TSA are applied.

Enhanced xylitol production: Expression of xylitol dehydrogenase from Gluconobacter oxydans and mixed culture of resting cell.

Xylitol has numerous applications in food and pharmaceutical industry, and it can be biosynthesized by microorganisms. In the present study, xdh gene, encoding xylitol dehydrogenase (XDH), was cloned from the genome of Gluconobacter oxydans CGMCC 1.49 and overexpressed in Escherichia coli BL21. Sequence analysis revealed that XDH has a TGXXGXXG NAD(H)-binding motif and a YXXXK active site motif, and belongs to the short-chain dehydrogenase/reductase family. And then, the enzymatic properties and kinetic parameter of purified recombinant XDH were investigated. Subsequently, transformations of xylitol from d-xylulose and d-arabitol, respectively, were studied through mixed culture of resting cells of G. oxydans wild-type strain and recombinant strain BL21-xdh. We obtained 28.80 g/L xylitol by mixed culture from 30 g/L d-xylulose in 28 h. The production was increased by more than three times as compared with that of wild-type strain. Furthermore, 25.10 g/L xylitol was produced by the mixed culture from 30 g/L d-arabitol in 30 h with a yield of 0.837 g/g, and the max volumetric productivity of 0.990 g/L h was obtained at 22 h. These contrast to the fact that wild-type strain G. oxydans only produced 8.10 g/L xylitol in 30 h with a yield of 0.270 g/g. To our knowledge, these values are the highest among the reported yields and productivity efficiencies of xylitol from d-arabitol with engineering strains.