Crystals in Minutes: Instant On‐Site Microcrystallisation of Various Flavours of the CYP102A1 (P450BM3) Haem Domain

Despite CYP102A1 (P450BM3) representing one of the most extensively researched metalloenzymes, crystallisation of its haem domain upon modification can be a challenge. Crystal structures are indispensable for the efficient structure‐based design of P450BM3 as a biocatalyst. The abietane diterpenoid derivative N‐abietoyl‐l ‐tryptophan (AbiATrp) is an outstanding crystallisation accelerator for the wild‐type P450BM3 haem domain, with visible crystals forming within 2 hours and diffracting to a near‐atomic resolution of 1.22 Å. Using these crystals as seeds in a cross‐microseeding approach, an assortment of P450BM3 haem domain crystal structures, containing previously uncrystallisable decoy molecules and diverse artificial metalloporphyrins binding various ligand molecules, as well as heavily tagged haem‐domain variants, could be determined. Some of the structures reported herein could be used as models of different stages of the P450BM3 catalytic cycle.     

Discovery of the First 2- State in 16C via Neutron Knockout Reaction

The ¹⁶C nucleus has been investigated by the neutron knockout reaction of ¹⁷C on a liquid hydrogen target. Applying the invariant mass method in inverse kinematics and γ-ray spectroscopy, the energy spectrum was reconstructed by triple-coincidence measurement, in which neutrons, charged fragments, and γ rays from the decay of the reaction residue (¹⁶C*) were detected. A peak at 0.47 MeV was observed in the invariant mass spectrum in coincidence with a peak at 0.74 MeV in the γ-ray spectrum, which indicates the presence of an unbound state with an excitation energy of 5.46 MeV. Comparison of the experimental cross section with the value derived by a theoretical calculation provided evidence that the spin-parity of this state is 2^?.     

Dynamic Investigation of Mechanism of Catalytic Reactions as Revealed by Spectroscopic Techniques

The study of chemisorption of gases on catalyst surfaces is of primary importance in elucidating the mechanism of heterogeneous catalysis. Accordingly, the adsorption of each of the gases which participate in the catalysis has been studied separately in many cases. However, chemisorption on the catalyst surface during the progress of reaction, generally speaking, cannot be estimated from the adsorption equilibrium of reactants and products measured separately for each species, but depends upon the mechanism of the reaction, the interaction among the adsorbed species, the formation of reaction intermediates or surface complexes, and the area of active region on the surface.     

Beta-decay study of Tz = - 2 proton-rich nucleus 24Si

$ \beta$ -decay spectroscopy on a T _z = - 2 proton-rich nucleus ²⁴Si was performed. The decay scheme of ²⁴Si was reconstructed by the $ \beta$ -delayed $ \gamma$ -ray and proton measurements. Two $ \beta$ branches to the bound 1₁ ⁺ and 1₂ ⁺ states in ²⁴Al were observed for the first time. The observation of the allowed transition firmly established the spin-parity assignment for the 1₂ ⁺ states. The branching ratios to the 1₁ ⁺ and 1₂ ⁺ states were determined to be 31(4)% and 23.9(15)%, respectively. The branching ratios to three unbound states in ²⁴Al including a new level at 6.735MeV were also determined for the first time. The level structure of ²⁴Al was compared with its mirror nucleus ²⁴Na . The Thomas-Ehrman shift on the 1₂ ⁺ state indicates s -wave dominance in the state as well as a characteristic behavior of the weakly bound s -wave proton in ²⁴Al .     

Hydrogenation of N‐Acylcarbamates and N‐Acylsulfonamides Catalyzed by a Bifunctional [Cp*Ru(PN)] Complex

Awakening of the Cp one : The bifunctional complex 1 facilitates the interaction with substrates bearing less electrophilic carbon atoms than ketones, epoxides, and imides. The title reaction was applicable to the reduction of Evans' asymmetric alkylation products to the chiral alcohols along with good recovery of the chiral oxazolidinone auxiliary. EWG=electron‐withdrawing group.

     

Hyperfine interaction of13O and23Mg implanted in Pt

The spin relaxation timeT ₁ for short-lived beta emitters¹³O and²³Mg implanted in Pt have been measured for the first time;T ₁T¹³O) = 2.90 ±0.65 Ks andT ₁ T(²³Mg) = 1665 ±140 Ks. The Knight shift for¹³O in Pt was measured at 300 K to beK(¹³O) = +(4.23 ±0.14) × 10^–3. In the case of¹³O, the Knight shift is unusually large and the relaxation time is unusually fast compared with other interstitial impurities in Pt. A KKR band-structure calculation reproduces the present large Knight shift fairly well.     

Development of palladium(II)-catalyzed oxidative cyclization of olefinic keto and/or lactone esters

A highly efficient palladium-catalyzed oxidative cyclization of olefinic keto and/or lactone esters, which features a catalytic cyclization employing one atmosphere of oxygen as a reoxidizing agent, is developed.     

Charge–discharge performances of Li–S battery using NaI–NaBH4–LiI solid electrolyte

Journal of Solid State Electrochemistry - In this study, Li–S batteries were fabricated using 9(15NaI∙NaBH4)∙LiI as the solid electrolyte, and their charge–discharge...     

Photoinduced metal-to-insulator transition in a manganite thin film

A persistent photoinduced metal-to-insulator transition has been confirmed in a manganite thin film, Pr_(0.55)(Ca_(0.75)Sr_(0.25))_(0.45)MnO3, near a multicritical point by monitoring with transport measurements and x-ray photoemission spectroscopy. Together with the previously reported reverse effect, the photoinduced insulator-to-metal transition, it is found that the relative stability of the metallic and insulating phases interchanges around 80 K in the middle of a very wide hysteresis loop, which is a manifestation of the large potential barrier due to the long-range elastic energy. It is shown that photons are much more effective in overcoming the barrier via the electronically excited intermediate states than via the heat mode.