Results 161 to 170 of about 12,023 (209)
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Sieve-tube proteins from Cucurbita maxima
Planta, 1974The two main proteins from the phloem exudate of Cucurbita maxima Duchesne have been isolated by ammonium-sulfate precipitation, DEAE-cellulose chromatography, and gel filtration, and have been characterized. They comprise about 40% each of the total protein. The amino-acid composition of these two proteins has been determined.
J, Beyenbach, C, Weber, H, Kleinig
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2018
Cucurbita maxima Duchesne Artbeschreibung: Ähnlich wie C. pepo, aber Blätter nicht oder nur wenig geteilt, mit stumpfen Zipfeln und Buchten, Blütenstiele rund, Früchte stets kugelig bis turbanförmig, Durchmesser 10-80 cm, meist gelb bis orange. Blütezeit: 6-9 Standort und Verbreitung in der Schweiz: Kultiviert / kollin / Verbreitung global: Stammt aus ...
Konrad Lauber +2 more
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Cucurbita maxima Duchesne Artbeschreibung: Ähnlich wie C. pepo, aber Blätter nicht oder nur wenig geteilt, mit stumpfen Zipfeln und Buchten, Blütenstiele rund, Früchte stets kugelig bis turbanförmig, Durchmesser 10-80 cm, meist gelb bis orange. Blütezeit: 6-9 Standort und Verbreitung in der Schweiz: Kultiviert / kollin / Verbreitung global: Stammt aus ...
Konrad Lauber +2 more
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Antigenotoxic spinasterol from Cucurbita maxima flowers
Mutation Research/Environmental Mutagenesis and Related Subjects, 1996The antigenotoxic constituent of squash flowers was isolated by solvent partitioning and repeated vacuum liquid chromatography. The micronucleus test, an in vivo method, was used to monitor the antigenotoxicity of the various fractions during the isolation process.
I M, Villaseñor +3 more
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Ascorbate oxidase from Cucurbita maxima
Phytochemistry, 1981Abstract Ascorbate oxidase is present in homogenates of the flesh of Cucurbita maxima fruits.
Luiz Bezerra Carvalho +2 more
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Different AT-rich satellite DNAs in Cucurbita pepo and Cucurbita maxima
Theoretical and Applied Genetics, 1986The AT-rich highly repeated satellite DNA of Cucurbita pepo (zucchini) and Cucurbita maxima (pumpkin) were cloned and their DNA structure was investigated. DNA sequencing revealed that the repeat length of satellite DNA in Cucurbita pepo is 349-352 base pairs. The percentage of AT-base pairs is about 61%.
M, Ganal, V, Hemleben
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Metabolic networks of Cucurbita maxima phloem
Phytochemistry, 2003Metabolomic analysis aims at a comprehensive characterization of biological samples. Yet, biologically meaningful interpretations are often limited by the poor spatial and temporal resolution of the acquired data sets. One way to remedy this is to limit the complexity of the cell types being studied. Cucurbita maxima Duch.
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Ornithine transaminase from Cucurbita maxima cotyledons
Phytochemistry, 1973Abstract During germination a marked increase in both soluble and particulate ornthine transaminase occurs in pumpkin cotyledons. Both enzymes had a pH optimum of 8.3 and a requirement for ornthine and α-ketoglutarate. Other keto acids or amino donors showed little activity.
W.E. Splittstoesser, L. Fowden
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KARAKTERISTIKE BUČA Cucurbita maxima
2015U ovom istraživanju su korišteni uzorci dviju buča Cucurbita maxima (Hokkaido i Kabocha) čiji ekstrakti su pripremani u dvije akademske godine: 2014/2015. i 2013/2014. Prošlogodišnji uzorci bili su podvrgnuti ekstrakciji uz refluksiranje i ekstrakciji u ultrazvučnoj kupelji. Fenolni spojevi svih uzoraka buča određeni su pomoću Folin-Ciocalteu metode, a
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Cucurbitacin 19-hydroxylase in Cucurbita maxima
Phytochemistry, 1978Abstract The enzymatic hydroxylation of the C-19-methyl group of cucurbitacin B and D was observed in partly purified preparations obtained from the unripe fruit of Cucurbita maxima . Assay methods were developed and the pH optimum, cofactor requirements, and substrate specificity determined.
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Phloemprotein bei Cucurbita maxima
Berichte der Deutschen Botanischen Gesellschaft, 1976ZusammenfassungDie basischen P‐proteine von Cucurbita maxima zeigen Glucansynthetase‐Aktivität. Sie werden offensichtlich ständig in den Geleitzellen neu gebildet und notwendigerweise wieder abgebaut. Ein Zusammenhang zwischen Verstopfung der Siebporen mit P‐protein‐Filamenten und Callosebildung ist zu erkennen.
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