In trans-1,3-butadiene, the ultrafast relaxation from the doubly excited state 2(1)Ag and the corresponding recovery of the ground state 1(1)Ag were observed simultaneously for the first time by time-resolved photoelectron spectroscopy (TRPES) using 29.5 eV high harmonic pulses. The fast recovery of 1(1)Ag shows that the following dissociation upon photoexcitation takes place after returning to the ground state. At 427 fs after photoexcitation, only the ionization energy from the C═C σ bond was found to remain shifted. Accompanying theoretical calculations with an assumption of Koopmans' theorem show that the ionization energy of the C═C σ bond is modulated by vibrational excitation of the antisymmetric C═C stretching mode. TRPES by high harmonics can probe the changes in the molecular structure sensitively.

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Using 42 nm high harmonic pulses, the dissociation dynamics of 1,2-butadiene was investigated by time-resolved photoelectron spectroscopy (TRPES), enabling us to observe dynamical changes of multiple molecular orbitals (MOs) with higher temporal resolution than conventional light sources. Because each lower-lying occupied MO has particular spatial electron distribution, the structural dynamics of photochemical reaction can be revealed. On the femtosecond time scale, a short-lived excited state with a lifetime of 37 ± 15 fs and the coherent oscillation of the photoelectron yield stimulated by Hertzberg-Teller coupling were observed. Ab initio molecular dynamics simulations in the electronically excited state find three relaxation pathways from the vertically excited structure in S1 to the ground state, and one of them is the dominant relaxation pathway, observed as the short-lived excited state. On the picosecond time scale, the photoelectron yields related to the C-C bond decreased upon photoexcitation, indicating C-C bond cleavage.

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Details of the properties of protease associated with matrix vesicle (M. V.) were studied. Bovine epiphyseal cartilage M. V. fraction according to Ali et al. were further fractionated by Percoll density gradient centrifugation by a modified method of Vaananen et al.. Most of the acid phosphatase was removed by Sephacryl S-200 gel filtration. Alkaline phosphatase and protease activities were effectively seperated by deoxycholate (0.008 %) treatment followd by Sephadex G-100 gel filtration. This protease fraction showed a 900 times higher specific activity than the Percoll fraction, optimal pH 6.5 against casein, single band on 7 % acrylamide gel electrophoresis and complete inhibition with 0.1 mM EDTA and o-phenanthlorine. Analysis of the digested proteoglycan on Sepharose CL-4B showed that this protease degrades proteoglycan as a trypsin-like mode. It is highly possible that the growth of hydroxyapatite microcrystal inside of M. V. may puncture the M. V. membrane and release the protease which promotes crystal formation at the calcification front.

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