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  • General Chemistry  (110)
  • thema EDItEUR::N History and Archaeology::NH History  (14)
  • Saccharomyces cerevisiae
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  • 1
    ISSN: 1432-0983
    Schlagwort(e): β-glucosidase ; Kluyveromyces fragilis ; DNA sequence ; Saccharomyces cerevisiae
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary The complete nucleotide sequence of the β-glucosidase gene of Kluyveromyces fragilis has been determined. This sequence contains an open reading frame of 2535 base pairs encoding a protein of 845 amino acids. Analysis of the transcription products revealed only one transcript of about 3 kb identical in both Kluyveromyces fragilis and in the expression host Saccharomyces cerevisiae. The protein molecular weight of 93,811 Kd deduced from the sequence is consistent with the 90,000 Kd determined by SDS polyacrylamide gel electrophoresis with the purified protein. Mapping of the starts of transcription shows that two starting points are used in the natural host Kluyveromyces fragilis. A comparison of the amino acid sequence with that of other β-glucosidases revealed three regions of homology. One of these regions contains an amino acid sequence very similar to a peptide isolated from the active site of β-glucosidase A3 from Aspergillus wentii and could be implicated in the catalytic mechanism of these glucolytic enzymes.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1434-1948
    Schlagwort(e): Metallocenes ; Hydroselenide ligands ; Selenium ; Se coordination chemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reactions of [Cp#2NbBH4] (1) [Cp# = C5Me5 (Cp*) or C5Me4Et] and [Cp′2TaH3] (Cp′ = tBuC5H4) with elemental selenium give complexes of the general composition [Cp2MSe2H]. These exist in three isomeric forms, A-C, depending on the metal and the chalcogen. [Cp#2NbSe2H] (2) incorporates the novel η2-Se2H ligand (C), which is labile when exposed to light. Solutions of 2(Cp*) can be converted into [Cp*2NbSe2H] (3), which exists in two isomeric forms A or B, along with [Cp*2NbSe3H] (4) and [Cp*2NbO2H] (5). [Cp′2Ta(η2-Se2)H] (6) is the only isomer found for the Ta system. Se abstraction by means of P(OEt)3 gives [Cp′2Ta(=Se)H] (7). Complex 7 can be reduced with Na/Hg and subsequently hydrolysed to give [Cp′2Ta(SeH)H2] (8), which has also been observed during the formation of 6. Coordination of [W(CO)5THF] at the Se lone pair of 7 affords the heterobimetallic complex 9. All compounds have been characterized by means of 1H- and, in some cases, 77Se-NMR spectroscopy. Products 8 and 9 have also been subjected to X-ray diffraction analysis.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 0947-6539
    Schlagwort(e): esters ; helical structures ; lanthanides ; luminescence ; tridentate ligands ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ligand diethyl pyridine-2, 6-dicarboxylate (L5) reacts with LnIII in acetonitrile to successively give the complexes [Ln(L5)i]3+ (Ln = La to Lu, i = 1-3). Spectroscopic investigations (ES-MS, UV/Vis, NMR) show that the 1:3 complexes [Ln(L5)3]3+ have poor stability in solution and exist as a mixture of rapidly interconverting conformers. Variable-temperature NMR data show that the helical P→M interconversion and dynamic on-off equilibria of the ester side arms both control the observed average structure in solution. Contrary to similar lanthanide building blocks possessing benzimidazole or carboxamide side arms, [Eu(L5)3]3+ has a sizable quantum yield in anhydrous acetonitrile; this has been attributed to an improved ligand → EuIII energy transfer resulting from a good energetic match between the ligand- and metal-centered excited states. Pure 1:3 complexes cannot be isolated in the solid state, but crystalline 1:2 complexes [Ln(L5)2](TfO)3.nH2O have been prepared. The X-ray crystal structure of [Eu(L5)2(TfO)2(OH2)]TfO (1) reveals two meridionally tricoordinated ligands L5, but the long Eu-O(ester) bonds imply only weak interactions between the carbonyl groups of the ester side arms and EuIII, providing a limited protection of the metallic site. The photophysical studies show that nonacoordinate EuIII in 1 binds an additional water molecule to give a decacoordinate complex in the solid state, thus confirming the accessibility of the metallic site for further complexation.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    ISSN: 0947-6539
    Schlagwort(e): carboxamides ; helical structures ; lanthanides ; luminescence ; tridentate ligands ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The ligand N,N,N',N'-tetra-ethylpyridine-2,6-dicarboxamide (L9) reacts with trivalent lanthanide ions (LnIII) to give stable mononuclear triple-stranded helical complexes [Ln(L9)3]3+ (Ln = La to Lu). The crystal and molecular structures of [La(L9)3](ClO4)3.2.5C2H5CN (8) and [Eu(L9)3](TfO)3.2THF (9) show that the three ligand strands are each meridionally tricoordinated to produce a pseudo-tricapped trigonal prismatic arrangement of the nine donor atoms (six amide O and three pyridine N) around LnIII. The distortions in the LaIII coordination sphere of 8 are more significant than for EuIII in 9, and the photophysical studies on Eu-doped (2%) La, Gd, and Lu complexes confirm a better structural match of L9 for the heavy LnIII ions. The separation of contact and pseudo-contact contributions to the induced lanthanide paramagnetic NMR shifts in [Ln(L9)3]3+ shows that the triple-helical structure is maintained in acetonitrile, but a minor structural change relative to that observed in the solid state occurs between TbIII and ErIII leading to two distinct isostructural series for Ln = La-Tb and Ln = Er-Lu. The origin of this effect together with its consequences for the dynamic helical (P→M) interconversion and stability of [Ln(L9)3]3+ in solution are discussed. A detailed investigation of the emission properties of [Ln(L9)3]3+ (Ln = Eu, Tb) shows that mixed pyridine-carboxamide ligands can be used to simultaneously optimize the structural and photophysical properties in mononuclear triple-helical lanthanide building blocks.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2417-2423 
    ISSN: 1434-193X
    Schlagwort(e): Nucleosides, 2′-C-methylene ; 2-C-Acetoxymethyl furanoid glycal ; π-Allyl palladium complex ; Ribonucleotide diphosphate reductase ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Two new routes to 2′,3′-dideoxy-2′-C-methylene nucleoside analogs have been developed. The first is based upon the coupling reaction of a 1-O-acetyl 2-C-(methylphenylsulfinyl) sugar with a silylated base under Vorbrüggen conditions, followed by thermal elimination of phenylsulfinic acid. The second route involved a condensation of a silylated base with a (π-allyl)palladium complex derived from a 2-C-acetoxymethyl furanoid glycal.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    ISSN: 1432-0983
    Schlagwort(e): Saccharomyces cerevisiae ; Yeast vectors ; Cosmids ; nif genes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Two vectors, termed pG63.11 (7.6 Kb) and pHCG3 (9.6 Kb), suitable for yeast transformation have been constructed. The pHCG3 vector has cosmid properties. Both vectors contain a single 3.3 Kb EcoRI-HindIII fragment of yeast origin which carries the yeast URA3 gene (1.1 Kb) and the origin of replication of the 2 µm plasmid (2.2 Kb). They confer ampicillin resistance and they contain 5 unique EcoRI,HpaI,HindIII,BamHI and SalI restriction sites. Cosmid pHCG3 was used to clone the nitrogen fixation (nif) gene cluster of Klebsiella pneumoniae carried by twoHindIII fragments of 17 and 26 Kb, respectively. The resulting cosmid, termed pGPC875 (53 Kb) which conferred a Nif+ phenotype to Escherichia coli, was introduced in yeast by transformation. No acetylene reduction activity was detectable in the transformants. However it was shown that the entire information for nitrogen fixation can be replicated and maintained intact in yeast for more than 50 generations of growth.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    ISSN: 1617-4623
    Schlagwort(e): RNA splicing ; Maturase ; Recombinase ; Mitochondria ; Saccharomyces cerevisiae
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary When the bI4 RNA maturase, encoded by the fourth intron of the mitochondrial cytochrome b gene of Saccharomyces cerevisiae, was expressed in Escherichia coli, formation of intra-chromosomal Lac+ recombinants was stimulated threefold. This “hyper-rec” phenotype was recA as well as recBCD dependent. The most active form of the bI4 maturase stimulated homologous recombination whereas splicing deficient mutants of bI4 maturase were either deficient in or unable to stimulate homologous recombination.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    ISSN: 1617-4623
    Schlagwort(e): Saccharomyces cerevisiae ; Transcription factor ; Zinc finger ; Multidrug resistance
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract TheSaccharomyces cerevisiae PDR3 gene, located near the centromere of chromosome II, has been completely sequenced and characterised. Mutationspdr3-1 andpdr3-2, which confer resistance to several antibiotics can be complemented by a wild-type allele of the PDR3 gene. The sequence of the wild-typePDR3 gene revealed the presence of a long open reading frame capable of encoding a 976-amino acid protein. The protein contains a single Zn(II)2Cys6 binuclear-type zinc finger homologous to the DNA-binding motifs of other transcriptional activators from lower eukaryotes. Evidence that the PDR3 protein is a transcriptional activator was provided by demonstrating that DNA-bound LexA-PDR3 fusion proteins stimulate expression of a nearby promoter containing LexA binding sites. The use of LexA-PDR3 fusions revealed that the protein contains two activation domains, one localised near the N-terminal, cysteine-rich domain and the other localised at the C-terminus. The salient feature of the PDR3 protein is its similarity to the protein coded byPDR1, a gene responsible forpleiotropicdrugresistance. The two proteins show 36% amino acid identity over their entire length and their zinc finger DNA-binding domains are highly conserved. The fact that the absence of both PDR1 and PDR3 (simultaneous disruption of the two genes) enhances multidrug sensitivity strongly suggests that the two transcriptional factors have closely related functions.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    ISSN: 1434-193X
    Schlagwort(e): Conformation analysis ; Electrochemistry ; Nitrogen heterocycles ; Dimerization ; Mechanism ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In aqueous media the one-electron reduction of the title compounds on a mercury pool generally gives rise to three dimers, which are distinguishable by HPL chromatography. From spectroscopic analyses it has been possible to propose a structure for these conformers and their stability has been studied. Two conformers are unstable, yielding the third conformer. A mechanism is proposed for this transformation.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    ISSN: 1434-193X
    Schlagwort(e): Transglycosylation ; Glycosidases ; Thermus thermophilus ; Carbohydrates ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: -The aim of this paper is to test the ability of a β-glycosidase from Thermus thermophilus to catalyse transglycosylation reactions in the presence of nitrophenyl glycosides as donors and other monosaccharides as acceptors. Our results show that this enzyme is able to induce such reactions either with nitrophenylgalactosides, -glucosides and -fucosides. With the two former donors, the autocondensation of the donor, which thus acts also as an acceptor, is faster than the transglycosylation with other acceptors. Furthermore, as the regioselectivity of the reactions is mainly of the β-[1→3] type, good yields are obtained for the synthesis of 2-nitrophenyl-β-D-galactopyranosyl-[1→3]-β-D-galactopyranoside and 2-nitrophenyl-β-D-glucopyranosyl-[1→3]-β-D-glucopyranoside. Conversely, in the presence of p-nitrophenylfucoside, the autocondensation is very limited, and with methyl-α-D-galactoside as an acceptor, the regioselectivity is mainly of the β-[1→6]-type resulting in the synthesis of methyl-β-D-fucopyranosyl-[1→6]-α-D-galactopyranoside.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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