Bringmann, Gerhard and Lang, Gerhard and Maksimenka, Katja and Hamm, Andreas and Gulder, Tobias A. M. and Dieter, Anke and Bull, Alan T. and Stach, James E.M. and Kocher, Niko and Muller, Werner E. G. and Fiedler, Hans-Peter (2005) Gephyromycin, the first bridged angucyclinone, from Streptomyces griseus strain NTK 14. Phytochemistry, 66 (11). pp. 1366-1373. ISSN 0031-9422 . (doi:https://doi.org/10.1016/j.phytochem.2005.04.010 ) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) ...
Streptomyces griseus subsp. griseus bacteriophage 22653 ATCC ® 11984-B1™ Designation: 22653 TypeStrain=False Application:
To study the inhibition mechanism of the native propeptide for the S. griseus trypsinogen, especially the role of the residue proline, we carried out molecular dynamics. Molecular dynamics (18) of the recombinants were simulated by the NAMD software with the CHARMM force field (http://www.ks.uiuc.edu/Research/namd) and comparatively analyzed with the active S. griseus trypsin (PDB ID, 1SGT). Total electrostatic energy in a particle mesh Ewald periodic box was calculated by the Ewald summation method, and the whole system was minimized using the descent method plus the conjugate gradient method. As shown in Fig. 4A, the major features of native trypsin were characterized. First, three disulfide bonds between residues C168 and C182, residues C191 and C220, and residues C42 and C58 held the substrate binding pocket rigid, and the correct fold was observed. Second, three hydrogen (H) bonds among the catalytic triad (H57, D102, and S195) maintained the accurate conformation of the catalytic center ...
The production of streptomycin using Streptomyces griseus using two types of chitin as a substrate was studied using a variety of fermentation techniques. Commercial chitin was obtained (Sigma) and comprised chemically purified crab shell. Pre-fermented chitin was the solid product from the lactic acid fermentation of shrimp waste using Lactobacillus paracasei A3. Bioassay, HPLC and FTIR methods were developed during this project for the quantification of streptomycin both in liquid phase and adsorbed on solid chitin surfaces. Shake flask experiments were carried out to determine basic production kinetics, as well as to establish if commercial and pre-fermented chitins produced different quantities of streptomycin. Shake flasks were also used to evaluate any effect of chitin concentration on streptomycin production. A range of submerged fermentations were undertaken in a standard 2 L bioreactor fitted with Rushton Turbines, at chitin concentrations from 0.4 %w/v to 10 %w/v, to study the effect ...
Streptomyces griseus EshA protein: developmentally regulated protein, required for sporogenic hyphal branches in Streptomyces griseus; amino acid sequence in first source
ID B1VQ72_STRGG Unreviewed; 299 AA. AC B1VQ72; DT 20-MAY-2008, integrated into UniProtKB/TrEMBL. DT 20-MAY-2008, sequence version 1. DT 10-APR-2019, entry version 33. DE SubName: Full=Uncharacterized protein {ECO:0000313,EMBL:BAG17173.1}; GN OrderedLocusNames=SGR_344 {ECO:0000313,EMBL:BAG17173.1}; OS Streptomyces griseus subsp. griseus (strain JCM 4626 / NBRC 13350). OC Bacteria; Actinobacteria; Streptomycetales; Streptomycetaceae; OC Streptomyces. OX NCBI_TaxID=455632 {ECO:0000313,EMBL:BAG17173.1, ECO:0000313,Proteomes:UP000001685}; RN [1] {ECO:0000313,EMBL:BAG17173.1, ECO:0000313,Proteomes:UP000001685} RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RC STRAIN=JCM 4626 / NBRC 13350 {ECO:0000313,Proteomes:UP000001685}; RX PubMed=18375553; DOI=10.1128/JB.00204-08; RA Ohnishi Y., Ishikawa J., Hara H., Suzuki H., Ikenoya M., Ikeda H., RA Yamashita A., Hattori M., Horinouchi S.; RT Genome sequence of the streptomycin-producing microorganism RT Streptomyces griseus IFO 13350.; RL J. Bacteriol. ...
Detail záznamu - tmRNA of Streptomyces collinus and Streptomyces griseus during the growth and in the presence of antibiotics - Detail záznamu - Knihovna Akademie věd České republiky
TY - JOUR. T1 - Oxidative/heat stress enhanced production of chitosanase from Streptomyces griseus cells through its interaction with liposome. AU - Ngo, Kien Xuan. AU - Umakoshi, Hiroshi. AU - Ishii, Haruyuki. AU - Bui, Huong Thi. AU - Shimanouchi, Toshinori. AU - Kuboi, Ryoichi. N1 - Funding Information: The fundamental concept of this study was supported by the Research Group of Membrane Stress Biotechnology. It was supported in part by a Grant-in-Aid for Scientific Research (No. 17656268, 19656203, 19656220, 20360350, and 21246121) from the Ministry of Education, Science, Sports, and Culture of Japan, a grant from the 21st Century COE program Creation of Integrated EcoChemistry and the Global COE program Bio-Environmental Chemistry of the Japan Society for the Promotion of Science (JSPS). The authors are grateful to the Research Center for Solar Energy Chemistry of Osaka University and the Gas hydrate Analyzing System of Osaka University. K. X. Ngo and H. T. Bui acknowledge financial ...
Biosynthesis of streptomyces griseus phage deoxyribonucleic acid by Judith Ann Shearer; 1 edition; First published in 1968; Subjects: DNA, Bacteriophages
p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.,/p> ,p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.,/p> ,p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).,/p> ,p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x,sup>64,/sup> + x,sup>4,/sup> + x,sup>3,/sup> + x + 1. The algorithm is described in the ISO 3309 standard. ,/p> ,p class=publication>Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.,br /> ,strong>Cyclic redundancy and other checksums,/strong>,br /> ,a href=http://www.nrbook.com/b/bookcpdf.php>Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993),/a>),/p> Checksum:i ...
1CP7: Interactions of Streptomyces griseus aminopeptidase with a methionine product analogue: a structural study at 1.53 A resolution.
ID B1VKL9_STRGG Unreviewed; 119 AA. AC B1VKL9; DT 20-MAY-2008, integrated into UniProtKB/TrEMBL. DT 20-MAY-2008, sequence version 1. DT 18-JUL-2018, entry version 26. DE SubName: Full=Uncharacterized protein {ECO:0000313,EMBL:BAG16864.1}; GN OrderedLocusNames=SGR_35t {ECO:0000313,EMBL:BAG16864.1}, SGR_7104t GN {ECO:0000313,EMBL:BAG23931.1}; OS Streptomyces griseus subsp. griseus (strain JCM 4626 / NBRC 13350). OC Bacteria; Actinobacteria; Streptomycetales; Streptomycetaceae; OC Streptomyces. OX NCBI_TaxID=455632 {ECO:0000313,EMBL:BAG16864.1, ECO:0000313,Proteomes:UP000001685}; RN [1] {ECO:0000313,EMBL:BAG16864.1, ECO:0000313,Proteomes:UP000001685} RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RC STRAIN=JCM 4626 / NBRC 13350 {ECO:0000313,Proteomes:UP000001685}, and RC NBRC 13350 {ECO:0000313,EMBL:BAG16864.1}; RX PubMed=18375553; DOI=10.1128/JB.00204-08; RA Ohnishi Y., Ishikawa J., Hara H., Suzuki H., Ikenoya M., Ikeda H., RA Yamashita A., Hattori M., Horinouchi S.; RT Genome sequence of the ...
Streptomyces griseus aminopeptidase has been characterized to have a dinuclear active site and to follow a dinuclear hydrolytic mechanism by means of activity assay, optical, and NMR spectroscopy. A sequential binding of Co2+ to the dinuclear sites in 20 mM Mes buffer at pH 6.1 has also been established. The results from these studies suggest that the two metal sites have a five-coordination sphere, with at least one coordinated His each. A di-Cu2+-substituted derivative of the enzyme has been prepared which exhibits a H-1 NMR spectrum with sharp hyperfine-shifted signals, again indicating the presence of a dinuclear active site. This H-1 NMR spectrum with sharp hyperfine-shifted features represents a first of its kind for a di-Cu2+ center in metalloproteins. Reprint in PDF (Read a short introduction about aminopeptidase) (Read abstract about NMR study of di-Cu(II)-aminopeptidase from Aeromonas ...
Selective incorporation of non-natural amino acid residues into proteins is a powerful approach to delineate structure-function relationships. Although many methodologies are available for chemistry-based protein engineering, more facile methods are needed to make this approach suitable for routine laboratory practice. Here, we describe a new strategy and provide a proof of concept for engineering semi-synthetic proteins. We chose a serine protease Streptomyces griseus trypsin (SGT) for this study to show that it is possible to efficiently couple a synthetic peptide containing a catalytically critical residue to a recombinant fragment containing the other active site residues. The 223-residue hybrid SGT molecule was prepared by fusing a chemically synthesized N-terminal peptide to a large C-terminal fragment of recombinant origin using native chemical ligation. This C-terminal polypeptide was produced from full-length SGT by cyanogen bromide cleavage at a genetically engineered Met57 position. ...
The structures of CBM5 domains have been elucidated for an endoglucanase, CBDEGZ from Erwinia chrysanthemi (EcEGZCBM5) and two chitinases ChBDChiB from Serratia marcescens (SmChiBCBM5) and ChBDChiC from Streptomyces griseus HUT6037 (SgChiCCBM5) [1, 2, 5]. The three structures revealed that CBM5 is composed of five β-strands (β1-5). The β1, β2 and β3 forms the principle structure and the additional short β-strands (β4 and β5) form an antiparallel β-sheet which is independent of the main strand (Figure 1). The EcEGZCBM5 resembles a ski-boot or L-shaped structure composed of only β-sheets [5]. Helix structures have not been found in CBM5 modules. There are a few differences in CBM5 modules of endo-glucanases (EcEGZCBM5) and chitinases (SmChiBCBM5 and SgChiCCBM5). The EcEGZCBM5 possesses a conserved disulfide bond between Cys4 and Cys61. These disulfide bonds have not been reported in SmChiBCBM5 and SgChiCCBM5. CBM5 modules possess surface exposed aromatic residues which interact with ...
The structures of CBM5 domains have been elucidated for an endoglucanase, CBDEGZ from Erwinia chrysanthemi (EcEGZCBM5) and two chitinases ChBDChiB from Serratia marcescens (SmChiBCBM5) and ChBDChiC from Streptomyces griseus HUT6037 (SgChiCCBM5) [1, 2, 5]. The three structures revealed that CBM5 is composed of five β-strands (β1-5) [1, 2, 5]. The β1, β2 and β3 forms the principle structure and the additional short β-strands (β4 and β5) form an antiparallel β-sheet which is independent of the main strand (Figure 1). The EcEGZCBM5 resembles a ski-boot or L-shaped structure composed of only β-sheets [5]. Helix structures have not been found in CBM5 modules. There are a few differences in CBM5 modules of endo-glucanases (EcEGZCBM5) and chitinases (SmChiBCBM5 and SgChiCCBM5). The EcEGZCBM5 possesses a conserved disulfide bond between Cys4 and Cys61 [5]. These disulfide bonds have not been reported in SmChiBCBM5 and SgChiCCBM5 [1, 2]. CBM5 modules possess surface exposed aromatic residues ...
Streptomycin is an aminocyclitol-aminoglycoside antibiotic produced by Streptomyces griseus. Streptomycin consists of aminocyclitol (streptidine), 6-deoxyhexose (streptose), and N-methyl-L-glucosamine moieties, which are formed by independent biosynthetic pathways. All of the moieties are derived from D-glucose. The streptidine moiety is synthesized via myo-inositol, which is then oxidized at C-1 and transaminated to give scyllo-inosamine. After phosphorylation, the compound is transamidinated by arginine. The same procedure is repeated at the C-3 position. The streptose moiety is made from D-glucose via a dTDP-glucose pathway. The exact biosynthetic route for the N-methyl-L-glucosamine moiety is unknown, though the biosynthetic gene cluster have been proposed ...
Cycloheximide is an antibiotic substance isolated from streptomycin-producing strains of Streptomyces griseus. Cycloheximide acts by inhibiting elongation during protein synthesis.
cansSAR 3D Structure of 5N3F | CAMP-DEPENDENT PROTEIN KINASE A FROM CRICETULUS GRISEUS IN COMPLEX WITH FRAGMENT LIKE MOLECULE N-[3-(AMINOMETHYL)PHENYL]ACETAMIDE | 5N3F_A | cAMP-dependent protein kinase catalytic subunit alpha - Also known as KAPCA_CRIGR, PRKACA. Phosphorylates a large number of substrates in the cytoplasm and the nucleus. Regulates the abundance of compartmentalized pools of its regulatory subunits through phosphorylation of PJA2 which binds and ubiquitinates these subunits, leading to their subsequent proteolysis. Phosphorylates CDC25B, ABL1, NFKB1, CLDN3, PSMC5/RPT6, PJA2, RYR2, RORA and VASP. RORA is activated by phosphorylation. Required for glucose-mediated adipogenic differentiation increase and osteogenic differentiation inhibition from osteoblasts. Involved in the regulation of platelets in response to thrombin and collagen; maintains circulating platelets in a resting state by phosphorylating proteins in numerous platelet inhibitory pathways when in complex with NF-kappa-B
The bacterial aminopeptidase isolated from the extracellular extract of Streptomyces griseus (SGAP) is a double-zinc exopeptidase with a high preference for large hydrophobic amino-terminus residues. It is a monomer of a relatively low molecular weight (30 kDa), is heat-stable, displays a high and efficient catalytic turnover and its activity is modulated by calcium ions. Several free amino acids were found to inhibit the activity of SGAP in the millimolar concentration range and can therefore serve for the study of binding of both inhibitors and reaction products. The current study is focused on the X-ray crystallographic analysis of the SGAP complexes with L-tryptophan and p-iodo-L-phenylalanine, both at 1.30 A resolution. These two bulky inhibitory amino acids were found to bind to the active site of SGAP in very similar positions and orientations. Both of them bind to the two active-site zinc ions via their free carboxylate group, while displacing the zinc-bound water/hydroxide that is ...
Cycloheximide is a eukaryote protein synthesis inhibitor, produced by the bacterium Streptomyces griseus. Cycloheximide exerts its effect by interfering with the translocation step in protein synthesis (movement of two tRNA molecules and mRNA in relation to the ribosome), thus blocking translational elongation. Cycloheximide is widely used in biomedical research to inhibit protein synthesis in eukaryotic cells studied in vitro (i.e. outside of organisms). It is inexpensive and works rapidly. Its effects are rapidly reversed by simply removing it from the culture medium.[1] Due to significant toxic side effects, including DNA damage, teratogenesis, and other reproductive effects (including birth defects and toxicity to sperm[2]), cycloheximide is generally used only in in vitro research applications, and is not suitable for human use as a therapeutic compound. Although it has been used as a fungicide in agricultural applications, this application is now decreasing as the health risks have become ...
S-412 96 Göteborg, Sweden Abstract The metal binding and activation of the dinuclear aminopeptidase from Streptomyces griseus has been studied by means of metal titration, kinetics, and thermodynamics using Cd2+ as a probe. Cd2+ binds to the two metal-binding sites in a sequential manner to produce a highly active Cd2+-substituted derivative, particularly in the presence of Ca2+. The first stepwise affinity constant for the binding of metal to the dinuclear metal-binding site was found to determine the selectivity, regardless of the second stepwise affinity constant. Although the selectivity of Cd2+ binding to this enzyme is not as great as Co2+, it is nevertheless similar to Zn2+ binding. Moreover, Ca2+ was found to significantly affect the metal binding and activation, inhibition, and entropy of activation of this enzyme. Reprint in PDF ...
Tarentino AL, Maley F. 1975. A comparison of the substrate specificities of endo-beta-N-acetylglucosaminidases from Streptomyces griseus and Diplococcus Pneumoniae.. Biochem Biophys Res Commun. 67(1):455-62. ...
Human CYP3A4 fused to its electron donor CPR was inactive, but capable of binding substrates identified in yeast expression studies. Plant CYP71B1:CPR fusion and Streptomyces griseus CYP105D1 were able to bind the varied xenobiotics studied and were active in the metabolism of a range of compounds. This suggested that Acinetobacter contained an electron donor system able to support the activity of CYP105D1 ...
The M3WT5 cell line was derived by transfecting CHO-K1 cells (ATCC CCL-61) with the pSVL expression vector containing the gene for the rat m3 muscarinic acetylcholine receptor.
Forms part of a macromolecular complex that catalyzes the attachment of specific amino acids to cognate tRNAs during protein synthesis. Modulates the secretion of AIMP1 and may be involved in generation of the inflammatory cytokine EMAP2 from AIMP1.
Time-lapse microscopy of a spreading control Cho-K1 cell expressing RLC-D,D-GFP (a phospho-mimetic mutant of the RLC) on fibronectin. The arrow poin...
Chinese Hamster Ovary (CHO) cells were metaphase-arrested with colcemid, exposed to hypotonic salt to swell the cells and chromosomes, fixed, embedded...
Metaphase-arrested CHO cells were swollen in 75 mM KCL, fixed with formaldehyde, post-fixed with OsO4, embedded, and 0.25 micron sections examined by ...
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The protein encoded by this gene is a member of the SEC22 family of vesicle trafficking proteins. It seems to complex with SNARE and it is thought to play a role in the ER-Golgi protein trafficking. This protein has strong similarity to Mus musculus and Cricetulus griseus proteins.[provided by RefSeq, Sep 2009 ...
Watch Dr. David Okun, a California-based oncologist, testifyi for the defense and conclude that there is not enough medical evidence to establish that the smoker suffered from primary lung cancer as opposed to cancer that began elsewhere and metastasized to the lungs.
Alignment of SsgA orthologues. Only those SsgA protein sequences have been used as input that are derived from species with known phenotype in submerged culture
Celebrate Government Meeting Professionals Month Wow! Can you remember what it was like when we were together at NEC? One day soon, we will be together again! October is Government Meeting Pro...
S. griseus mutant NP4, which was isolated by UV mutagenesis, showed a bald and wrinkled colony morphology because of ectopic septation in substrate hyphae and subsequent spore formation. The ectopic spores were the same as aerial spores in size, thickness of the spore wall, and shape, as determined by transmission and scanning electron microscopy, and in heat and lysozyme susceptibility. Mutant NP4 also formed abundant spores in liquid medium, whereas the parental strain IFO13350 rarely forms submerged spores under these conditions. The wall of the ectopic spores is supposed to be thicker than those of the submerged spores formed by several Streptomyces spp., including S. griseus B-2682 (32), under specific conditions, because the spores of NP4 were resistant to lysozyme. We therefore assume that both on solid and in liquid medium, mutant NP4 forms two separate cross walls in the vegetative hyphae and matures each compartment into a spore indistinguishable from aerial spores in many aspects, as ...
IDENTIFICATION AND USE: streptomycin is an antibiotic produced by the soil actinomycete Streptomyces griseus. It acts by inhibiting the initiation and elongation processes during protein synthesis. Streptomycin is an Aminoglycoside Antibacterial and Antimycobacterial. The chemical classification of streptomycin is Aminoglycosides.. Streptomycin is a broad-spectrum aminoglycoside antibiotic typically used for treatment of active tuberculosis, always in combination with other antituberculosis agents. Streptomycin is usually used in combination with agents that are known to be hepatotoxic and the role of streptomycin in liver injury has been difficult to assess, but most information suggests that streptomycin is not hepatotoxic.. HUMAN EXPOSURE/TOXICITY: intravenous and intramuscular therapy with streptomycin has been linked to mild and asymptomatic elevations in serum alkaline phosphatase, but therapy rarely affects aminotransferase levels or bilirubin and changes typically resolve rapidly once ...
Streptomycin Sulfate is a water-soluble antibacterial originally antiseptic from Streptomyces griseus. Streptomycin Sulfate acts by bounden to the 30S subunit of the bacterial ribosome arch to inhibition of protein amalgam and afterlife in affected bacteria. Streptomycin Sulfate is awful alive adjoin gram-negative with some action adjoin gram-positive bacteria. Gibco® Streptomycin Sulfate is acclimated abandoned or…
15112992] Biosynthesis of the antitumor chromomycin A3 in Streptomyces griseus: analysis of the gene cluster and rational design of novel chromomycin analogs. (Chem Biol. , 2004 ...
Streptomycin, antibiotic synthesized by the soil organism Streptomyces griseus. Streptomycin was discovered by American biochemists Selman Waksman, Albert Schatz, and Elizabeth Bugie in 1943. The drug acts by interfering with the ability of a microorganism to synthesize certain vital proteins. It
1) Two extracellular staphylolytic enzymes have been Isolated and purified from submerged cultures of Streptomyces griseus. 2) The enzymes were electrophoretically homogeneous at several pH values. A single peak was obtained for each protein on ultracentrifugation. Based on gel-filtration molecular weights of 11,800 and 13,000 were determined for enzyme 1 and enzyme 2 respectively. 3) The ionic strength and pH optima for lytic activity of the two enzymes against staphylococcal cells and their isolated cell walls have been detenained. The effects of several cations and certain known enzyme inhibitors have been tested on lytic action of the two enzymes against cell walls. 4) Both enzymes were N-acetylhexosaminidases. Examination of the acid hydrolysis products of fully digested cell walls treated with naBH4 demonstrated that both enzymes were muramidases. 5) Both enzymes caused lysis to varying extents, of the cell walls of a range of gram positive organisms. However, E. coli, the only gram ...
We investigated the effect of proteases, widely used for neuron isolation in electrophysiological studies, on the amplitude and kinetic characteristics of persistent sodium current (INaP) in hippocampal CA1 pyramidal neurons. Properties of INaP were studied on neurons isolated by mechanical treatment (control group) and by mechanical and enzymatic treatment using pronase E (from Streptomyces griseus) or protease type XXIII (from Aspergillus oryzae). We show that in neurons isolated with pronase E kinetic of activation and density of INaP was unaltered. Enzymatic treatment with protease type XXIII did not alter INaP activation but result in significant decrease in INaP density. Our data indicates that enzymatic treatment using pronase E for neuron isolation is preferable for investigation of INaP ...
The present investigation was aimed at the synthesis of 2-mercaptobenzoxazole, a series of Schiffs bases 1-[α-(arylidine hydrazino) acetyl]-2-mercaptobenzoxazole 2MB-2a-e and 2-[(aryl)-3-(acetyl amino)-1, 3-thiazolidine-4-ones]-2-mercaptobenzoxazole 2MB-3a have been synthesized from 2-mercaptobenzoxazole and compounds were screened for their antibacterial and antifungal activities by agar diffusion method. The structures of the all synthesized compounds have been determined by their IR, 1H NMR and elemental analysis. All the compounds have showed moderate to promising antibacterial and antifungal activities, against Gram-positive bacterium Bacillus subtilis (MTCC 441), Streptomyces griseus (MTCC 1540) and Gram-negative bacterium Escherichia coli (MTCC 443) and for antifungal activity against Ashbya gossypii (MTCC 358) and Aspergillus niger (MTCC 282).. [PDF] , ...
An inshore bottom-dwelling shark found down to at least 51 m (Compagno et al. 2005); Also dwells in semi-enclosed sea areas with sand bottom. Teshima (1981) studied the reproduction of this species in Japanese waters and report that females mature at 68-76 cm total length (TL) and reach a maximum size of 107.9 cm TL; males at 70-75 cm TL (Teshima 1981), and reach a maximum size of 91.2 cm TL. Compagno et al. (2005) report that females reach maturity at about 80 cm TL and males at 62-71 cm TL. Mating takes place in July, followed by a gestation period of about 10 months in Japanese waters, parturition in April-May (Teshima 1981, Compagno et al. 2005, Yamaguchi et al. 2006). Reproduction is viviparous, with a yolk-sac placenta (Teshima 1981, D.A. Ebert pers. obs.). Females give birth to 2-20 pups in April-June, and size at birth is 28-30 cm TL (Teshima 1981, Compagno et al. 2005, Yamaguchi et al. 2006). Probably feeds on benthic invertebrates, especially crustaceans (D.A. Ebert pers. obs.). This ...
General Care: 25-35°C, 60-70% rel. humidity Feeding: bramble, Asclepias spp., bittersweet nightshade Breeding: oviposition into substrate (humus-sand-soil) Advice/Specifics: roost at night at more protected and humid places (e.g. under bark ...
Accepted name: glutamine scyllo-inositol transaminase. Reaction: L-glutamine + 2,4,6/3,5-pentahydroxycyclohexanone = 2-oxoglutaramate + 1-amino-1-deoxy-scyllo-inositol. Other name(s): glutamine scyllo-inosose aminotransferase; L-glutamine-keto-scyllo-inositol aminotransferase; glutamine-scyllo-inosose transaminase; L-glutamine-scyllo-inosose transaminase. Systematic name: L-glutamine:2,4,6/3,5-pentahydroxycyclohexanone aminotransferase. Comments: A pyridoxal-phosphate protein.. Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 9033-03-8. References: 1. Walker, J.B. and Walker, M.S. Streptomycin biosynthesis. Transamination reactions involving inosamines and inosadiamines. Biochemistry 8 (1969) 763-770. [PMID: 5781017]. ...
Taxonomy of the species Streptomyces bambergiensis Wallhäusser et al. 1966 (Approved Lists 1980) pro synon. Streptomyces prasinus Ettlinger et al. 1958 (Approved Lists 1980) emend. Labeda et al. 2016
This species appears to be restricted to southeast Africa to the Arabian Sea, including the Red Sea and Persian Gulf. Junior synonyms Plectorhinchus unicolor (Macleay, 1883) and Plectorhinchus griseus (Cuvier, 1830) are considered valid according to Johnson et al., 2015 (Ref. 103290). Species record and information will be repaired accordingly.. ...
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Streptomyces:Media_and_Solutions/Antibiotic_&_Resistance_Marker_Information , Antibiotic & Resistance Marker Information]] ,, There is a problem with the this link in the dewikified version, hence the & in the file name was changed to and ...
bacterial SgpA protein: genes sgpA, sgpB & sgpC encode three different proteins that constitute sulfur globule envelope in many bacteria; amino acid sequence in first source
The muraymycins, a family of nucleoside-lipopeptide antibiotics, were purified from the extract of Streptomyces sp. LL-AA896. The… Expand ...
Back to VLAN Membership, now that ports 1 to 12 belong to 2 vlan 1 and 180, we will select vlan 1 at VLAN Identifier and remove the U (Untag) symbols at the bottom of the ports 1 to 12 in vlan 1 ...