Streptomyces spinoverrucosus | |
---|---|
Scientific classification | |
Domain: | Bacteria |
Phylum: | Actinomycetota |
Class: | Actinomycetia |
Order: | Streptomycetales |
Family: | Streptomycetaceae |
Genus: | Streptomyces |
Species: | S. spinoverrucosus |
Binomial name | |
Streptomyces spinoverrucosus Diab and Al-Gounaim 1982 [1] | |
Type strain | |
163MA, ATCC 33692, Diab 163 MA, DSM 41648, IFO 14228, IFO 14250, JCM 5077, KCC S-1077, KCCS-1077, LMG 20321, MS, MS 1488, NBRC 14228, NBRC 14250, NCIB 11666, NCIMB 11666, NRRL B-16932 [2] |
Streptomyces spinoverrucosus is a bacterium species from the genus of Streptomyces which has been isolated from air in Kuwait. [1] [3] [4] [5] Streptomyces spinoverrucosus produces salinazinone A, salinazinone B, galvaquinone A, galvaquinone B, galvaquinone C, spithioneine A, spithioneine B and anthraquinones. [6] [7] [8] [9]
Meldrum's acid or 2,2-dimethyl-1,3-dioxane-4,6-dione is an organic compound with formula C6H8O4. Its molecule has a heterocyclic core with four carbon and two oxygen atoms; the formula can also be written as [−O−(C 2)−O−(C=O)−(CH2)−(C=O)−].
For the parent molecule 9,10-anthraquinone, see anthraquinone
Bohemic acid is a mixture of chemical compounds which is obtained through fermentation by actinobacteria species in the genus Actinosporangium (Actinoplanaceae). The name honors the Puccini opera La Bohème and many individual components of the acid carry the names of characters from La Bohème. Most of those components are antitumor agents and anthracycline antibiotics active against Gram-positive bacteria.
Aspergillusenes are a group of chemical compounds first isolated from a strain of sea fan-derived fungus Aspergillus sydowii. They are sesquiterpenes of the bisabolane-type.
The Center for Pharmaceutical Research and Innovation (CPRI) is a University of Kentucky-based research center established by the University of Kentucky College of Pharmacy in 2012 to facilitate academic translational research and drug discovery/drug development. The UK CPRI specializes in natural product-based drug discovery from microbes found within unique environments including underground and surface coal mines, acid mine drainage and mine reclamation sites, thermal vents associated with underground coal mine fires and deep-well drilling for carbon sequestration. CPRI also provides core support for medicinal chemistry, assay development and screening, rational drug design, computational chemistry, and ADMET. The Center collaborates with investigators focused on drug discovery or development research in the areas of cancer, drug and alcohol addiction, cardiovascular disease, infectious disease, regenerative medicine and neurodegenerative disease.
Streptomyces bacillaris is a bacterium species from the genus of Streptomyces which has been isolated from forest soil in Oregon in the United States.
Streptomyces griseoincarnatus is a bacterium species from the genus of Streptomyces which has been isolated from soil in Russia. Streptomyces griseoincarnatus produces erygrisin. Streptomyces griseoincarnatus produces variapeptin, citropeptin, and ammosamide D.
Streptomyces lusitanus is a bacterium species from the genus of Streptomyces which has been isolated from soil. Streptomyces lusitanus produces 7-chlortetracycline, naphthyridinomycin, cyanocycline B, N-desmethylnaphthyridinomycin and tetracycline.
Streptomyces netropsis is a bacterium species from the genus of Streptomyces. Streptomyces netropsis produces the antibiotics netropsin and distamycin A and the antifungal polyene mycoheptin.
Streptomyces nigrescens is a bacterium species from the genus of Streptomyces which has been isolated from soil. Streptomyces nigrescens produces 5-alkyl-1,2,3,4-tetrahydroquinolines and the antibiotics phoslactomycin A - F.
Streptomyces seoulensis is a bacterium species from the genus of Streptomyces which has been isolated from soil from Korea. Streptomyces seoulensis produces lipoamide dehydrogenase.
Streptomyces xiamenensis is a bacterium species from the genus of Streptomyces which has been isolated from mangrove sediments in Xiamen in the Fujian Province in China. Streptomyces xiamenensis produces the antifibrotic drug xiamenmycin.
Streptomyces xinghaiensis is a bacterium species from the genus of Streptomyces which has been isolated from marine sediments from Xinghai Bay near Dalian in China.
Erythrobacter is a Gram-negative and rod-shaped bacteria genus from the family Erythrobacteraceae.
Tsukamurella pulmonis is a Gram-positive and aerobic bacterium from the genus Tsukamurella which has been isolated from the sputum from a patient with lung tuberculosis in Germany.
4-Quinolone is an organic compound derived from quinoline. It and 2-quinolone are the two most important parent quinolones. 4-Quinolone exists in equilibrium with a minor tautomer, 4-hydroxyquinoline (CAS#611-36-9). Aside from pedagogical interest, 4-quinolone is of little intrinsic value but its derivatives, the 4-quinolone antibiotics, represent a large class of important drugs.
Naphtholactam is an organic compound derived from naphthalene. It is a tricyclic species consisting of a naphthalene core fused with a lactam (NH-CO-) at the 1,8-positions. The N-alkyl derivatives are commercially important.
Enterocin and its derivatives are bacteriocins synthesized by the lactic acid bacteria, Enterococcus. This class of polyketide antibiotics are effective against foodborne pathogens including L. monocytogenes, Listeria, and Bacillus. Due to its proteolytic degradability in the gastrointestinal tract, enterocin is used for controlling foodborne pathogens via human consumption.
Tetrahydroxanthones are natural products formally derived by partial reduction of xanthone. They are produced by various fungi, bacteria, and plants. Some are precursors to larger xanthone natural products. One example is neosartorin, composed of 5-acetylblennolide A and blennolide C, exhibits antibacterial activity against Gram-positive bacteria, notably including Staphylococcus aureus.
Mono-N-protected amino acid (MPAA) is a bifunctional ligand that plays a key role in C–H functionalizations by accelerating the reaction rate and imparting specified chirality into the product. Amino acids are ideal building blocks for chiral ligand synthesis due to the cost, accessibility, large variety, solubility, and inherent chirality. Naturally occurring amino acids are transformed into chiral MPAA ligands that, upon coordination to metal complexes, allow reactions to occur that are otherwise energetically unfavorable. Great strides in the development of MPAA ligands over the past two decades have led to the integral role that enantioselective catalysis now plays in complex organic synthesis.
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