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41.
Kazuyoshi Kawazu Jocelyn P. Alcantara Akio Kobayashi 《Bioscience, biotechnology, and biochemistry》2013,77(10):2719-2722
Two insecticidal compounds were isolated from the seeds of Annona squamosa. One was identified as annonin (squamocin) and the other was characterized as a novel dihydroxy-bistetrahydrofuran fatty acid lactone (acetogenin) with 35 carbons. These two compounds were toxic to eggs, larvae and adults of the fruitfly. 相似文献
42.
Ilexol, a new triterpenoid alcohol isolated from the barks of several species of the Genus Ilex, has now been oxidized with chromium trioxide to yield a ketone, designated as ilexone of C30H48O, m.p. 239.5–240.5°, and – 68.74°, which gives oxirne of m. p. 256.5–257.5°, 2,4-dinitrophenylhydrazone of m.p. 260–261°, and positive Zimmermann test.On reduction with sodium and ethanol as well as with lithium aluminum hydride, it has been shown that ilexone is regenerated to yield an alcohol proved to be identical with natural ilexol.On reduction according to the procedure of Huang-Minion, ilexone has been shown to yield an oxygen-free compound, designated as ilexene of C30H50, and m.p. 241–242°.It seems most likely that ilexol might be a triterpenoid alcohol of C30H49OH, an alcoholic hydroxyl group of which is secondary in nature, and moreover attached at C–3 in its molecule. 相似文献
43.
Vu Huu Thanh Kazuyoshi Okubo Kazuo Shibasaki 《Bioscience, biotechnology, and biochemistry》2013,77(7):1501-1503
Two kinds of N-acetylmuramidase, M-1 and M-2 enzymes, that were isolated from the cultural broth of Stm. globisporus 1829, were remarkably different in amino acid composition, immunological properties and modes of lytic action from each other. The M-1 enzyme was composed of 186 amino acid residues of which two moles were of half cystine, while the M-2 enzyme was composed of 99 amino acid residues with no cysteine. The hydrolyzing action of the M-2 enzyme was suppressed by the presence of an O-acetyl group on muramic acid residues in the peptidoglycan moiety, while that of the M-l enzyme was independent of the presence of O-acetyl groups. However, the hydrolyzing activity of both enzymes was enhanced when some muramic acid residues were substituted with stem peptides containing alanine, isoglutamine and lysine. 相似文献
44.
Keisuke Kitamura Kazuyoshi Okubo Kazuo Shibasaki 《Bioscience, biotechnology, and biochemistry》2013,77(5):1083-1085
Kinetics of the acyl transfer catalyzed by Xanthomonas α-amino acid ester hydrolase was studied. The enzyme hydrolyzed d-α-phenylglycine methyl ester (d-PG-OMe) to give equimolar amounts of d-α-phenylglycine and methanol. With d-PG-OMe as an acyl donor and 7-amino-3-deacetoxy-cephalosporanic acid (7-ADCA) as an acyl acceptor, the enzyme transferred the acyl group from d-PG-OMe to 7-ADCA in competition with water. The addition of amine nucleophiles (7-ADCA and 6-aminopenicillanic acid) decreased the molecular activity (ko) of the enzyme-catalyzed hydrolysis of d-PG-OMe, whereas it did not alter the Michaelis constant (KM), and plots of l/ko against the initial concentration of a nucleophile (no) gave a straight line. These results support the assumptions that the overall process for hydrolysis and acyl transfer proceeds through a common acyl-enzyme intermediate, that the acylation step of the enzyme is rate-limiting, and that the transfer competes with the hydrolysis of the acyl donor. 相似文献
45.
Kim M Handley Nathan C VerBerkmoes Carl I Steefel Kenneth H Williams Itai Sharon Christopher S Miller Kyle R Frischkorn Karuna Chourey Brian C Thomas Manesh B Shah Philip E Long Robert L Hettich Jillian F Banfield 《The ISME journal》2013,7(4):800-816
Stimulation of subsurface microorganisms to induce reductive immobilization of metals is
a promising approach for bioremediation, yet the overall microbial community response is
typically poorly understood. Here we used proteogenomics to test the hypothesis that
excess input of acetate activates complex community functioning and syntrophic
interactions among autotrophs and heterotrophs. A flow-through sediment column was
incubated in a groundwater well of an acetate-amended aquifer and recovered during
microbial sulfate reduction. De novo reconstruction of community sequences
yielded near-complete genomes of Desulfobacter (Deltaproteobacteria),
Sulfurovum- and Sulfurimonas-like Epsilonproteobacteria and
Bacteroidetes. Partial genomes were obtained for Clostridiales
(Firmicutes) and Desulfuromonadales-like Deltaproteobacteria.
The majority of proteins identified by mass spectrometry corresponded to
Desulfobacter-like species, and demonstrate the role of this organism in
sulfate reduction (Dsr and APS), nitrogen fixation and acetate oxidation to CO2
during amendment. Results indicate less abundant Desulfuromonadales, and possibly
Bacteroidetes, also actively contributed to CO2 production via the
tricarboxylic acid (TCA) cycle. Proteomic data indicate that sulfide was partially
re-oxidized by Epsilonproteobacteria through nitrate-dependent sulfide oxidation
(using Nap, Nir, Nos, SQR and Sox), with CO2 fixed using the reverse TCA cycle.
We infer that high acetate concentrations, aimed at stimulating anaerobic heterotrophy,
led to the co-enrichment of, and carbon fixation in Epsilonproteobacteria.
Results give an insight into ecosystem behavior following addition of simple organic
carbon to the subsurface, and demonstrate a range of biological processes and community
interactions were stimulated. 相似文献
46.
Kentaro Kumoi Tadashi Satoh Kazuyoshi Murata Takeshi Hiromoto Tsunehiro Mizushima Yukiko Kamiya Masanori Noda Susumu Uchiyama Hirokazu Yagi Koichi Kato 《PloS one》2013,8(3)
Assembly of the eukaryotic 20S proteasome is an ordered process involving several proteins operating as proteasome assembly factors including PAC1-PAC2 but archaeal 20S proteasome subunits can spontaneously assemble into an active cylindrical architecture. Recent bioinformatic analysis identified archaeal PAC1-PAC2 homologs PbaA and PbaB. However, it remains unclear whether such assembly factor-like proteins play an indispensable role in orchestration of proteasome subunits in archaea. We revealed that PbaB forms a homotetramer and exerts a dual function as an ATP-independent proteasome activator and a molecular chaperone through its tentacle-like C-terminal segments. Our findings provide insights into molecular evolution relationships between proteasome activators and assembly factors. 相似文献
47.
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49.
Yoshikazu Furusawa Shinji Yamada Shunsuke Itai Takuro Nakamura Miyuki Yanaka Masato Sano Hiroyuki Harada Masato Fukui Mika K. Kaneko Yukinari Kato 《Biochemistry and Biophysics Reports》2019
Monoclonal antibodies (mAbs) against human, mouse, rat, rabbit, dog, cat, and bovine podoplanin (PDPN), a lymphatic endothelial cell marker, have been established in our previous studies. However, mAbs against horse PDPN (horPDPN), which are useful for immunohistochemical analysis, remain to be developed. In the present study, mice were immunized with horPDPN-overexpressing Chinese hamster ovary (CHO)-K1 cells (CHO/horPDPN), and hybridomas producing mAbs against horPDPN were screened using flow cytometry. One of the mAbs, PMab-219 (IgG2a, kappa), specifically detected CHO/horPDPN cells via flow cytometry and recognized horPDPN protein using Western blotting. Furthermore, PMab-219 strongly stained CHO/horPDPN via immunohistochemistry. These findings suggest that PMab-219 is useful for investigating the function of horPDPN. 相似文献
50.
Yukinari Kato Yoshikazu Furusawa Shinji Yamada Shunsuke Itai Junko Takei Masato Sano Mika K. Kaneko 《Biochemistry and Biophysics Reports》2019
Podoplanin (PDPN) is known as a lymphatic endothelial cell marker. Monoclonal antibodies (mAbs) against human, mouse, rat, rabbit, dog, cat, bovine, pig, and horse PDPN have been established in our previous studies. However, mAbs against alpaca PDPN (aPDPN), required for immunohistochemical analysis, remain to be developed. In the present study, we employed the Cell-Based Immunization and Screening (CBIS) method for producing anti-aPDPN mAbs. We immunized mice with aPDPN-overexpressing Chinese hamster ovary (CHO)-K1 cells (CHO/aPDPN), and hybridomas producing mAbs against aPDPN were screened using flow cytometry. One of the mAbs, PMab-225 (IgG2b, kappa), specifically detected CHO/aPDPN cells via flow cytometry and recognized the aPDPN protein on Western blotting. Further, PMab-225 strongly stained lung type I alveolar cells, colon lymphatic endothelial cells, and kidney podocytes via immunohistochemistry. These findings demonstrate that PMab-225 antibody is useful to investigate the function of aPDPN via different techniques. 相似文献