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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 756 (1995), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant pathology 54 (2005), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: To quantify the magnitude and the spatial spread of grapevine downy mildew secondary sporangia, 4685 Plasmopara viticola single lesion samples were collected from 18 plots spread across central Europe. Disease symptoms were collected on two to 22 sampling dates per plot between 2000 and 2002. Four multiallelic microsatellite markers were used for genotypic identification of pathogen samples. Genetic analysis showed more than 2300 site-specific P. viticola genotypes, indicating that populations are genetically rich demographic units. Approximately 70% of the genotypes were sampled once and 14% were sampled twice throughout the various epidemics. In the 18 populations only seven genotypes (0.3%) were identified more than 50 times. Three genotypes particularly successful in causing disease through secondary cycles showed mainly a clustered distribution. The distance of sporangial migration per secondary cycle was less than 20 m and their plot colonization rate was calculated at around 1–2 m2 day−1. Downy mildew epidemics of grapevine are therefore the result of the interaction of a multitude of genotypes, each causing limited (or a few) lesions, and of a dominant genotype able to spread stepwise at plot-scale. These findings contrast with current theories about grapevine downy mildew epidemiology, which postulate that there is massive vineyard colonization by one genotype and long-distance migration of sporangia.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Gene 99 (1991), S. 77-86 
    ISSN: 0378-1119
    Keywords: Arabidopsis ; Brassica ; Raphanus sativus ; Recombinant DNA ; embryogenesis ; rape ; signal peptide ; storage protein
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Plant Science Letters 35 (1984), S. 139-146 
    ISSN: 0304-4211
    Keywords: germination ; in vitro translation ; radish ; stored mRNA
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    BIT 21 (1981), S. 245-254 
    ISSN: 1572-9125
    Keywords: Foreign types ; Interfaces ; Modules ; Mixed languages ; Procedures ; Type checking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract As a support for writing software, a comprehensive set of problem oriented languages appears preferable to any so-called universal language, as soon as static checking is sufficient to ensure type correctness of the mixed language program. We lay the basis for a mixed language system where this requirement is fulfilled. The general outline of the system is first sketched. Detailed consideration is then given to our basic constructs for establishing communication between languages, namely “standard” types and “foreign” types. “Abstract” types, such as defined in CLU, are finally shown to be a particular class of “foreign” types.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Distributed computing 13 (2000), S. 29-43 
    ISSN: 1432-0452
    Keywords: Key words:Asynchronous distributed system – Checkpointing protocols – Fault-Tolerance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science
    Notes: Summary. A useless checkpoint is a local checkpoint that cannot be part of a consistent global checkpoint. This paper addresses the following problem. Given a set of processes that take (basic) local checkpoints in an independent and unknown way, the problem is to design communication-induced checkpointing protocols that direct processes to take additional local (forced) checkpoints to ensure no local checkpoint is useless. The paper first proves two properties related to integer timestamps which are associated with each local checkpoint. The first property is a necessary and sufficient condition that these timestamps must satisfy for no checkpoint to be useless. The second property provides an easy timestamp-based determination of consistent global checkpoints. Then, a general communication-induced checkpointing protocol is proposed. This protocol, derived from the two previous properties, actually defines a family of timestamp-based communication-induced checkpointing protocols. It is shown that several existing checkpointing protocols for the same problem are particular instances of the general protocol. The design of this general protocol is motivated by the use of communication-induced checkpointing protocols in “consistent global checkpoint”-based distributed applications such as the detection of stable or unstable properties and the determination of distributed breakpoints.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-2242
    Keywords: Arabidopsis thaliana ; Microsatellite ; Polymorphism ; PCR amplification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The major simple sequence repeats present in the Arabidopsis genome were identified by Southern hybridizations with 49 oligonucleotide probes matching all the possible combinations of motifs up to 4 nucleotides long. The method used allowed us to perform all the hybridizations under the same temperature conditions. A good correlation was observed with the data obtained from database analysis, indicating that the method can be useful for identifying the major classes of microsatellite loci in species for which few or no sequence data are available. AG/CT, AAG/CTT, ATG/CAT and GTG/CAC are the major motifs present in the Arabidopsis genome that can be used as convenient probes to isolate microsatellite loci by screening libraries. AAG/CTT is the more frequent of these motifs, and its relative frequency in Arabidopsis is much higher than averagely found in the plant kingdom. About 8% of the cDNA clones from an immature silique library contains AG/CT, AAG/CTT or ATG/CAT microsatellite loci. Several microsatellite loci were isolated by screening genomic and cDNA libraries. Twenty-six tri-nucleotide loci were PCR amplified from four different ecotypes, and polymorphism was observed for 12 of them; 10 loci showing two alleles and 2 loci showing three alleles.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1617-4623
    Keywords: Key wordsSaccharopolyspora erythraea ; Erythromycin biosynthetic genes ; Desosamine ; Mycarose ; Glycosyltransferase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The production of erythromycin A by Saccharopolysporaerythraea requires the synthesis of dTDP-D-desosamine and dTDP-L-mycarose, which serve as substrates for the transfer of the two sugar residues onto the macrolactone ring. The enzymatic activities involved in this process are largely encoded within the ery gene cluster, by two sets of genes flanking the eryA locus that encodes the polyketide synthase. We report here the nucleotide sequence of three such ORFs located immediately downstream of eryA, ORFs 7, 8 and 9. Chromosomal mutants carrying a deletion either in ORF7 or in one of the previously sequenced ORFs 13 and 14 have been constructed and shown to accumulate erythronolide B, as expected for eryB mutants. Similarly, chromosomal mutants carrying a deletion in either ORF8, ORF9, or one of the previously sequenced ORFs 17 and 18 have been constructed and shown to accumulate 3-α-mycarosyl erythronolide B, as expected for eryC mutants. The ORF13 (eryBIV ), ORF17 (eryCIV ) and ORF7 (eryBII ) mutants also synthesised small amounts of macrolide shunt metabolites, as shown by mass spectrometry. These results considerably strengthen previous tentative proposals for the pathways for the biosynthesis of dTDP-D-desosamine and dTDP-L-mycarose in Sac. erythraea and reveal that at least some of these enzymes can accommodate alternative substrates.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1617-4623
    Keywords: Key words Macrolides ; Glycosyltransferase ; Deoxyhexoses ; Actinomycetes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A 6-kb region from the chromosome of Streptomyces antibioticus, an oleandomycin producer, was cloned and sequenced. This region was located between the 3′ end of the gene encoding the third subunit of the oleandomycin type I polyketide synthase and the oleP and oleB genes, which encode a cytochrome P450 monooxygenase and an oleandomycin resistance gene, respectively. Analysis of the nucleotide sequence revealed the presence of five genes encoding a cytochrome P450-like protein (oleP1), two glycosyltransferases (oleG1 and oleG2) involved in the transfer of the two 6-deoxysugars (L-oleandrose and D-desosamine) to the oleandomycin macrolactone ring, a methyltransferase (oleM1), and a gene (oleY) of unknown function. Insertional inactivation of this region by gene disruption generated an oleandomycin non-producing mutant which accumulated a compound that, according to mass spectrometry analysis, could correspond to the oleandomycin macrolactone ring (oleandolide), suggesting that the mutation affects oleandrosyl glycosyltransferase.
    Type of Medium: Electronic Resource
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