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1.
Rapid Commun Mass Spectrom ; 15(14): 1229-38, 2001.
Article in English | MEDLINE | ID: mdl-11445907

ABSTRACT

Electrospray ionisation mass spectrometry (ESI-MS) has been used for the determination and quantitation of a broad range of 24 antibiotics, from groups including aminoglycosides, beta-lactams, tetracyclines, antifungals and glycopeptides. Spectra have been acquired for all 24 antibiotics derived from pure samples dissolved in acetonitrile/water, along with samples extracted from complex fermentation liquor. Quantitation was carried out by the detection of the protonated molecules, using time-scheduled single-ion monitoring (SIM). ESI-MS was used to detect and quantify to 5-microM levels. A one-step extraction of antibiotics with an organic solvent (methanol) was used for this rapid and simple procedure. Specificity is not matched by other methods and antibiotic analogues (e.g. the five forms of erythromycin) can be determined within minutes.


Subject(s)
Anti-Bacterial Agents/chemistry , Spectrometry, Mass, Electrospray Ionization/methods , Fermentation , Saccharopolyspora/physiology
2.
Trends Biotechnol ; 16(11): 483-9, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9830157

ABSTRACT

Penicillin production by Penicillium chrysogenum is not only commercially important but arguably the most intensively investigated secondary-metabolic pathway in fungi. Isolation of the structural genes encoding the three main penicillin-biosynthetic enzymes has stimulated the use of molecular approaches to optimize yield and permitted genetic analysis of current production strains, which are themselves the products of 50 years of strain and process improvement. Parallel studies on the penicillin-producing genetic model organism Aspergillus nidulans are now addressing questions about the genetic regulation of primary and secondary metabolism, the compartmentalization of biosynthesis and the excretion of the end products.


Subject(s)
Aspergillus nidulans/genetics , Aspergillus nidulans/metabolism , Penicillins/biosynthesis , Penicillium chrysogenum/genetics , Penicillium chrysogenum/metabolism , Gene Expression Regulation, Fungal , Mutation , Oxidation-Reduction , Species Specificity
4.
Mol Gen Genet ; 154(3): 311-8, 1977 Sep 09.
Article in English | MEDLINE | ID: mdl-144864

ABSTRACT

The extranuclear mitochondrial oligomycin-resistant mutation of Aspergillus nidulans, (oliA1), was transferred asexually into four nuclear oligomycin-resistant strains of different phenotypes. In all four cases, the possession of the nuclear plus extranuclear mutation led to an increase in the in vivo level of oligomycin resistance. In two cases, the altered cytochrome spectrum and impaired growth ability determined by (oliA1) were suppressed by the nuclear mutations. In the third case, the in vitro oligomycin resistance of the double mutant ATPase was dramatically increased above that of either of the component single mutant strains, indicating a synergystic interaction between the nuclear and extranuclear gene products. In the fourth case, the double mutant became cold-sensitive. A new extranuclear mitochondrial oligomycin-resistant mutation (oliB332) is described. This mutant is phenotypically similar to, though not identical with, (oliA1) but is separable by recombination. A range of nuclear oligomycin-resistant mutants have been mapped. Despite presenting five distinctly different phenotypes, they all map at the same locus.


Subject(s)
Aspergillus nidulans/drug effects , Genes , Mitochondria , Oligomycins/pharmacology , Adenosine Triphosphatases/metabolism , Aspergillus nidulans/enzymology , Chromosomes , Drug Resistance, Microbial , Extrachromosomal Inheritance , Translocation, Genetic
6.
J Bacteriol ; 125(2): 389-97, 1976 Feb.
Article in English | MEDLINE | ID: mdl-1107321

ABSTRACT

The cytochrome spectra of two extranuclear mutants of Aspergillus nidulans and the double-mutant recombinant formed from them have been examined both at room temperature and at the temperature of liquid N2 and compared with those of the wild-type strain. The oligomycin-resistant, slow growing mutant contained an increased amount of cytochrome c without any loss of cytochromes b and a,a3. The cold-sensitive mutant, apparently normal when grown at 37 C, showed an increased amount of cytochrome c and a partial loss of cytochromes b and a,a3 when grown at 20 C. A combination of these effects was observed in the double-mutant recombinant. Cyanide-resistant respiration was present in both mutant strains and in the recombinant at much higher levels than in the wild-type strain. In the oligomycin-resistant mutant, this was usually present together with cyanide-sensitive respiration, whereas in the cold-sensitive mutant and recombinant grown at 20 C cyanide-resistant approached 100%. Inhibitor and growth yield studies indicated that the cyanide-resistant pathway was not used by the cold-sensitive mutant during growth at 20 C.


Subject(s)
Aspergillus nidulans/metabolism , Cytochromes/biosynthesis , Extrachromosomal Inheritance , Mutation , Oxygen Consumption , Antimycin A/pharmacology , Aspergillus nidulans/drug effects , Aspergillus nidulans/growth & development , Cyanides/pharmacology , Drug Resistance, Microbial , Hydroxamic Acids/pharmacology , Mitochondria/metabolism , Oligomycins/pharmacology , Oxygen Consumption/drug effects , Recombination, Genetic , Temperature
7.
Mol Gen Genet ; 141(1): 69-79, 1975 Nov 03.
Article in English | MEDLINE | ID: mdl-765725

ABSTRACT

Two- and three-point extranuclear crosses have been carried out via heterokaryons involving the three extranuclear mitochondrial markers of Aspergillus nidulans: (oliA1), (cs67) and (camA112). All three markers appear to be located on a single functional mitochondrial genome. Recombination between all three pairs of extranuclear markers appears to be equally frequent, suggesting a lack of genetic linkage. An important feature of these results is the variable and often marked non-equality of frequency of reciprocal classes of recombinants.


Subject(s)
Aspergillus nidulans/physiology , Extrachromosomal Inheritance , Mitochondria , Recombination, Genetic , Gene Frequency , Genetic Linkage , Phenotype
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