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11.
12.
Günther Huber Otto Machhammer Maren Lepple Claudia Weidlich Cord-Henrich Dustmann Akane Hartenbach 《化学,工程师,技术》2021,93(4):664-672
A photovoltaic system could supply a single-family house with electrical power, warm water, and room heat if the energy would be distributed over the year to suit the load profile. However, storage systems for this are not state of the art yet. A concrete example is used to estimate which parameters such a power storage system should have. A suitable electrochemical reaction system based on inorganic salt mixtures is proposed. The German Federal Ministry of Education and Research is currently funding the development of a world storage facility based on the same reaction system. 相似文献
13.
Prof. Dr. Fumitaka Kudo Jiahao Zhang Shusuke Sato Dr. Akane Hirayama Prof. Dr. Tadashi Eguchi 《Chembiochem : a European journal of chemical biology》2019,20(19):2458-2462
Pactamycin is an antibiotic produced by Streptomyces pactum with antitumor and antimalarial properties. Pactamycin has a unique aminocyclitol core that is decorated with 3-aminoacetophenone, 6-methylsaliciate, and an N,N-dimethylcarbamoyl group. Herein, we show that the adenylation enzyme PctU activates 3-aminobenzoic acid (3ABA) with adenosine triphosphate and ligates it to the holo form of the discrete acyl carrier protein PctK to yield 3ABA-PctK. Then, 3ABA-PctK is N-glycosylated with uridine diphosphate-N-acetyl-d -glucosamine (UDP-GlcNAc) by the glycosyltransferase PctL to yield GlcNAc-3ABA-PctK. Because 3ABA is known to be a precursor of the 3-aminoacetophenone moiety, PctU appears to be a gatekeeper that selects the appropriate 3-aminobenzoate starter unit. Overall, we propose that acyl carrier protein-bound glycosylated 3ABA derivatives are biosynthetic intermediates of pactamycin biosynthesis. 相似文献
14.
NAD+‐Dependent Dehydrogenase PctP and Pyridoxal 5′‐Phosphate Dependent Aminotransferase PctC Catalyze the First Postglycosylation Modification of the Sugar Intermediate in Pactamycin Biosynthesis 下载免费PDF全文
Dr. Akane Hirayama Jinmiao Chu Ena Goto Dr. Fumitaka Kudo Prof. Dr. Tadashi Eguchi 《Chembiochem : a European journal of chemical biology》2018,19(2):126-130
The unique five‐membered aminocyclitol core of the antitumor antibiotic pactamycin originates from d ‐glucose, so unprecedented enzymatic modifications of the sugar intermediate are involved in the biosynthesis. However, the order of the modification reactions remains elusive. Herein, we examined the timing of introduction of an amino group into certain sugar‐derived intermediates by using recombinant enzymes that were encoded in the pactamycin biosynthesis gene cluster. We found that the NAD+‐dependent alcohol dehydrogenase PctP and pyridoxal 5′‐phosphate dependent aminotransferase PctC converted N‐acetyl‐d ‐glucosaminyl‐3‐aminoacetophonone into 3′‐amino‐3′‐deoxy‐N‐acetyl‐d ‐glucosaminyl‐3‐aminoacetophenone. Further, N‐acetyl‐d ‐glucosaminyl‐3‐aminophenyl‐β‐oxopropanoic acid ethyl ester was converted into the corresponding 3′‐amino derivative. However, PctP did not oxidize most of the tested d ‐glucose derivatives, including UDP‐GlcNAc. Thus, modification of the GlcNAc moiety in pactamycin biosynthesis appears to occur after the glycosylation of aniline derivatives. 相似文献
15.
Lysine‐241 Has a Role in Coupling 2OG Turnover with Substrate Oxidation During KDM4‐Catalysed Histone Demethylation 下载免费PDF全文
Dr. Rebecca L. Hancock Dr. Martine I. Abboud Dr. Tristan J. Smart Dr. Emily Flashman Dr. Akane Kawamura Prof. Christopher J. Schofield Dr. Richard J. Hopkinson 《Chembiochem : a European journal of chemical biology》2018,19(9):917-921
The JmjC histone lysyl demethylases (KDMs) play important roles in modulating histone methylation states and have the potential to be regulated by oxygen availability. Lys241 of the KDM4 subfamily is proposed to be important in oxygen binding by KDM4A. We report evidence that, although Lys241 is unlikely to be directly involved in oxygen binding, it has an important role in coupling 2‐oxoglutarate cosubstrate oxidation with lysine demethylase activity. The results suggest that compounds promoting the uncoupling of substrate oxidation are of interest as JmjC‐KDM inhibitors. 相似文献
16.
The synthesis of polypropylene (PP) oligomer—clay intercalation compounds was studied by using three kinds of PP oligomers and organophylic clay. PP oligomers were two types of maleic-anhydride-modified PP oligomers containing different amount of maleic anhydride groups and one type of hydroxy modified PP oligomer. Organophylic clay was sodium-ion-exchanged montmorillonite with octadecylammonium ion (C18—Mt). PP oligomer was mixed with C18—Mt at 200°C. Maleic-anhydride-modified PP oligomer, which was of high acid value type, and hydroxy-modified PP oligomer were intercalated between silicate layers of clay; and PP oligomer—clay intercalation compounds were synthesized successfully. But maleic-anhydride-modified PP oligomer, which was of low acid value type, was not intercalated. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 1781–1785, 1997 相似文献
17.
Shirasuna K Kobayashi A Nitta A Nibuno S Sasahara K Shimizu T Bollwein H Miyamoto A 《Reproduction (Cambridge, England)》2012,143(4):491-500
The development of the corpus luteum (CL), which secretes large amounts of progesterone to establish pregnancy, is accompanied by active angiogenesis, vascularization, and lymphangiogenesis. Negative feedback regulation is a critical physiological mechanism. Vasohibin-1 (VASH1) was recently discovered as a novel endothelium-derived negative feedback regulator of vascularization. We therefore investigated the expression of VASH1 in the bovine CL. Expression of VASH1 mRNA and protein was predominantly localized to luteal endothelial cells (LECs). VASH1 expression in the CL was constant through the early to late luteal phases and decreased during CL regression relating with the action of luteolytic prostaglandin F(2)(α) in vivo. To investigate the role of VASH1, we determined whether VASH1 treatment affects angiogenesis and/or lymphangiogenesis using LECs and lymphatic endothelial cells (LyECs) in vitro. Vascular endothelial growth factor A (VEGFA) stimulated the expression of VASH1 in LECs but not in LyECs, and VASH1 completely blocked VEGFA-induced formation of capillary-like tube structures of LECs and LyECs in vitro. In summary, VASH1 is predominantly located on LECs in the bovine CL and inhibits the angiogenic and lymphangiogenic actions of VEGFA. Bovine CL therefore has a VEGFA-VASH1 system that may be involved in regulation of luteal function, especially in the development of the CL. The results indicate that VASH1 has the potential to act as a negative feedback regulator of angiogenesis and lymphangiogenesis in the CL in cows. 相似文献
18.
Dr. Kyohei Muguruma Rento Osawa Akane Fukuda Naoto Ishikawa Konomi Fujita Dr. Akihiro Taguchi Dr. Kentaro Takayama Dr. Atsuhiko Taniguchi Prof. Yuji Ito Prof. Yoshio Hayashi 《ChemMedChem》2021,16(11):1814-1821
Immunoglobulin G (IgG)-binding peptides such as 15-IgBP are convenient tools for the site-specific modification of antibodies and the preparation of homogeneous antibody–drug conjugates. A peptide such as 15-IgBP can be selectively crosslinked to the fragment crystallizable region of human IgG in an affinity-dependent manner via the ϵ-amino group of Lys8. Previously, we found that the peptide 15-Lys8Leu has a high affinity (Kd=8.19 nM) due to the presence of the γ-dimethyl group in Leu8. The primary amino group required for the crosslinking to the antibodies has, however, been lost. Here, we report the design and synthesis of a novel unnatural amino acid, 4-(2-aminoethylcarbamoyl)leucine (Aecl), which possesses both the γ-dimethyl fragment and a primary amino group. A peptide containing Aecl8 (15-Lys8Aecl) was synthesized and showed a binding affinity ten times higher (Kd=24.3 nM) than that of 15-IgBP (Kd=267 nM). Fluorescein isothiocyanate (FITC)-labeled 15-Lys8Aecl with an N-hydroxy succinimide ester at the side chain of Aecl8 (FITC-15-Lys8Aecl(OSu)) successfully labeled an antibody (trastuzumab, Herceptin®) with the fluorophore. This peptide scaffold has both strong binding affinity and crosslinking capability, and could be a useful tool for the selective chemical modification of antibodies with molecules of interest such as drugs. 相似文献
19.
Akane Fujii Dr. Osamu Nakagawa Yuki Kishimoto Yusuke Nakatsuji Natsumi Nozaki Prof. Dr. Satoshi Obika 《Chembiochem : a European journal of chemical biology》2020,21(6):860-864
1,3-Diaza-2-oxophenoxazine (“phenoxazine”), a tricyclic cytosine analogue, can strongly bind to guanine moieties and improve π–π stacking effects with adjacent bases in a duplex. Phenoxazine has been widely used for improving duplex-forming abilities. In this study, we have investigated whether phenoxazine and its analogue, 1,3,9-triaza-2-oxophenoxazine (9-TAP), could improve triplex-forming abilities. A triplex-forming oligonucleotide (TFO) incorporating a phenoxazine component was found to show considerably decreased binding affinity with homopurine/homopyrimidine double-stranded DNA, so the phenoxazine system was considered not to function as either a protonated cytosine or thymine analogue. Alternatively, a 9-TAP-containing artificial nucleobase developed by us earlier as a new phenoxazine analogue functioned as a thymine analogue with respect to AT base pairs in a parallel triplex DNA motif. The fluorescence of the 9-TAP moiety was maintained even in triplex (9-TAP:AT) formation, so 9-TAP might be useful as an imaging tool for various oligonucleotide nanotechnologies requiring triplex formation. 相似文献
20.
Alessandro Narduzzo Amalia Coldea Arzhang Ardavan John Singleton Luca Pardi Vasile Bercu Akane Akutsu-Sato Hiroki Akutsu Scott Turner Peter Day 《Journal of Low Temperature Physics》2006,142(3-4):585-588
We report a spin resonance study of the family of quasi-two-dimensional organic (super)conductors β”-(BEDT-TTF)4[(H3O)M(C2O4)3]S, where M is a 3d transition metal ion and S is a host solvent molecule. The spin systems for M = Cr3+ (S = 3/2) and M = Fe3+ (S = 5/2) are investigated by means of both resonant and field modulation techniques in the frequency range between 50 and
313 GHz. The role of the different solvent molecules in determining the degree of spin-orbit coupling and the local symmetry
at the metal ion site is established. The low temperature behaviour of intensities, positions and widths of the resonant lines
shows significant modifications of the spin-orbit coupling, and of the inter-and intra-ionic spin-spin inter actions. Despite
the onset of a weak antiferromagnetic internal field at low temperature, the ultimate narrowing of the lines suggests spin-lattice
interactions may still be the dominant relaxation process. Diamagnetic screening in the mixed state of the superconducting
samples for fields parallel to the quasi-two-dimensional layers induces additional lineshifts only below B = 2.5T and T =
4K, determining the threshold of full field penetration within the anion layers. 相似文献