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Sphingomonas sp. strain P2, which is capable of utilizing phenanthrene as a sole carbon and energy source, was isolated from petroleum-contaminated soil in Thailand. Gas chromatography-mass spectrometry and (1)H and (13)C nuclear magnetic resonance analyses revealed two novel metabolites from the phenanthrene degradation pathway. One was identified as 5,6-benzocoumarin, which was derived by dioxygenation at the 1- and 2-positions of phenanthrene, and the other was determined to be 1,5-dihydroxy-2-naphthoic acid. Other metabolites from phenanthrene degradation were identified as 7, 8-benzocoumarin, 1-hydroxy-2-naphthoic acid and coumarin. From these results, it is suggested that strain P2 can degrade phenanthrene via dioxygenation at both 1,2- and 3,4-positions followed by meta-cleavage.

Here we demonstrate the controllability on morphology of hydrothermal ZnO nanowires through the critical concentration for nucleation. When Zn ion concentration is relatively low, the nucleation process preferentially occurs on the (0001) plane, promoting nanowire growth. In contrast, for relatively high Zn ion concentration, the (101¯0) plane emerges, suppressing nanowire growth. The occurrence of this nucleation competition on the crystal planes as a function of concentration is caused by differences in the critical nucleation sizes between the (0001) plane and the (101¯0) plane. Furthermore, we found that the density of ZnO nanowires trend to decrease with increasing the growth time due to the lateral growth effect. Photoluminescence measurement of ZnO nanowires exhibited that the near band emission peak of 380 nm decreased with decreasing nanowire diameter while the broad emission peak below band gap appears the opposite trend because of surface to volume ratio effect.