BIOMAT Database Logo BIOMAT Database Logo

Metabolic development and secondary biosynthesis in Penicillium urticae. 1965

J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith

UI MeSH Term Description Entries
D008055 Lipids A generic term for fats and lipoids, the alcohol-ether-soluble constituents of protoplasm, which are insoluble in water. They comprise the fats, fatty oils, essential oils, waxes, phospholipids, glycolipids, sulfolipids, aminolipids, chromolipids (lipochromes), and fatty acids. (Grant & Hackh's Chemical Dictionary, 5th ed) Lipid
D010407 Penicillium A mitosporic Trichocomaceae fungal genus that develops fruiting organs resembling a broom. When identified, teleomorphs include EUPENICILLIUM and TALAROMYCES. Several species (but especially PENICILLIUM CHRYSOGENUM) are sources of the antibiotic penicillin. Penicilliums
D010636 Phenols Benzene derivatives that include one or more hydroxyl groups attached to the ring structure.
D002247 Carbon Isotopes Stable carbon atoms that have the same atomic number as the element carbon but differ in atomic weight. C-13 is a stable carbon isotope. Carbon Isotope,Isotope, Carbon,Isotopes, Carbon
D003470 Culture Media Any liquid or solid preparation made specifically for the growth, storage, or transport of microorganisms or other types of cells. The variety of media that exist allow for the culturing of specific microorganisms and cell types, such as differential media, selective media, test media, and defined media. Solid media consist of liquid media that have been solidified with an agent such as AGAR or GELATIN. Media, Culture
D006019 Glycolysis A metabolic process that converts GLUCOSE into two molecules of PYRUVIC ACID through a series of enzymatic reactions. Energy generated by this process is conserved in two molecules of ATP. Glycolysis is the universal catabolic pathway for glucose, free glucose, or glucose derived from complex CARBOHYDRATES, such as GLYCOGEN and STARCH. Embden-Meyerhof Pathway,Embden-Meyerhof-Parnas Pathway,Embden Meyerhof Parnas Pathway,Embden Meyerhof Pathway,Embden-Meyerhof Pathways,Pathway, Embden-Meyerhof,Pathway, Embden-Meyerhof-Parnas,Pathways, Embden-Meyerhof
D000085 Acetates Derivatives of ACETIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the carboxymethane structure. Acetate,Acetic Acid Esters,Acetic Acids,Acids, Acetic,Esters, Acetic Acid
D012459 Salicylates The salts or esters of salicylic acids, or salicylate esters of an organic acid. Some of these have analgesic, antipyretic, and anti-inflammatory activities by inhibiting prostaglandin synthesis. Salicylate,Salicylic Acids,Acids, Salicylic
D013438 Sulfhydryl Compounds Compounds containing the -SH radical. Mercaptan,Mercapto Compounds,Sulfhydryl Compound,Thiol,Thiols,Mercaptans,Compound, Sulfhydryl,Compounds, Mercapto,Compounds, Sulfhydryl
D066298 In Vitro Techniques Methods to study reactions or processes taking place in an artificial environment outside the living organism. In Vitro Test,In Vitro Testing,In Vitro Tests,In Vitro as Topic,In Vitro,In Vitro Technique,In Vitro Testings,Technique, In Vitro,Techniques, In Vitro,Test, In Vitro,Testing, In Vitro,Testings, In Vitro,Tests, In Vitro,Vitro Testing, In

Related Publications

J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Conidiogenesis and secondary metabolism in Penicillium urticae.
January 1977, Applied and environmental microbiology,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
De novo biosynthesis of secondary metabolism enzymes in homogeneous cultures of Penicillium urticae.
February 1980, Journal of bacteriology,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Some observations on aromatic biosynthesis in Penicillium urticae Bainier.
January 1955, Experimental cell research,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Oxidases involved in biosynthesis of macrolide antibiotic patulolides from Penicillium urticae S11R59.
May 1989, The Journal of antibiotics,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
An ultrastructural examination of Penicillium urticae during the transition to antibiotic biosynthesis.
August 1986, Canadian journal of microbiology,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Manganese and antibiotic biosynthesis. I. A specific manganese requirement for patulin production in Penicillium urticae.
March 1986, Canadian journal of microbiology,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Manganese and antibiotic biosynthesis. III. The site of manganese control of patulin production in Penicillium urticae.
March 1986, Canadian journal of microbiology,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Isolation of tautomycetin as a regulator of secondary metabolite production for Penicillium urticae.
January 1995, Bioscience, biotechnology, and biochemistry,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
Malonate as a biosynthetic intermediate in Penicillium urticae.
June 1962, The Journal of biological chemistry,
J D Bu'Lock, and D Hamilton, and M A Hulme, and A J Powell, and H M Smalley, and D Shepherd, and G N Smith
New macrolides from Penicillium urticae mutant S11R59.
May 1986, The Journal of antibiotics,
Copied contents to your clipboard!