Schiffs bases and derived secondary amines as plant growth inhibitors

Seventy-two Schiffs bases, 44 corresponding secondary amines, and 12 N-acetylated compounds were tested on their growth activity. Eighty-one compounds were active as growth inhibitors in at least one of three bioassays.     

Anatomische und morphologische Untersuchungen an den Involucral- und Spreublättern von Compositen

Ohne Zusammenfassung     

Versuche zum Herbizideinsatz in gesäten Kohlarten

In den Jahren 1987 bis 1989 wurden die Auswirkungen und Effekte eines kombinierten Befalls des Winterweizens mit Sitobion avenae (Fabr.) und Puccinia recondita Rob.ex Desm. f.sp.tritici Erikss. untersucht. Dabei wurde das Verhalten der Schaderregerpopulationen und die Einflußnahme auf das Ertragsgeschehen bei separatem und simultanem Befall erfaßt. Während bei starkem Befall der oberen Blattetagen mit P.recondita eine Förderung der Aphidenpopulation an den Ähren der befallenen Pflanzen registriert werden konnte, war bei schwachem Braunrostbefall keine Einflußnahme auf die Blattläuse nachweisbar. Durch das kombinierte Auftreten beider Schaderreger kann es zu Reduktionen bei der Kornmasse/Ähre und bei der Tausendkornmasse kommen, die größer sind, als die Summe der Verluste bei Einzelbefall. Ähren stark braunrostbefallener Winterweizenpflanzen wurden zeitiger von S.avenae angeflogen und schneller besiedelt als diese von gesunden Kontrollpflanzen. Als Ursache für die Förderung der Populationsentwicklung von S.avenae werden durch P.recondita induzierte Veränderungen im Angebot an freien Aminosäuren in der Wirtspflanze diskutiert.     

Subunit polypeptide composition of rubisco and the origin of allopolyploid Arabidopsis suecica (Brassicaceae)

The polypeptide composition of the large and small subunits of Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) from Arabidopsis thaliana, A. suecica and Cardaminopsis arenosa have been studied by IEF (isoelectric focusing) analysis. The putative recent alopolyploid origin of A. suecica is supported. The chloroplast encoded large subunits served to identify solely A. thaliana as the maternal parent whereas the nuclear encoded small subunits indicate C. arenosa as the paternal species.     

Dna stability and survival of bacillus subtilis spores in extreme dryness

The inactivation of Bacillus subtilis spores during long-term exposure (up to several months) to extreme dryness (especially vacuum) is strain-dependent, through only to a small degree. During a first phase (lasting about four days) monolayers of spores lose about 20% of their viability, regardless of the strain studied. During this phase loss in viability can be equally attributed both to damages of hydrophobic structures (membranes and proteins) and DNA. During a second phase lasting for the remaining time of experimental observation (weeks, months and years) the loss in viability is slowed. A viability of 55% to 75% (depending on the strain) is attained after a total exposure of 36 days. The loss in viability during the second phase can be correlated with the occurrence of DNA double strand breaks. Also covalent DNA-protein cross-links are formed by vacuum exposure. If the protein moiety of these cross-links is degraded by proteinase K-treatment in vitro additional DNA double strand breaks result. The data are also discussed with respect to survival on Mars and in near Earth orbits.     

Identification of mitochondrial proteins on two-dimensional electrophoresis gels of extracts of adult Drosophila melanogaster

Several hundred proteins have been resolved on two-dimensional gels of extracts of [³⁵S]methionine-labeled adult Drosophila melanogaster. 27 of these polypeptides disappear from the gel pattern after feeding the K⁺ ionophore nonactin. These proteins have been identified as mitochondrial, since the two-dimensional gel pattern of extracts of isolated mitochondria correlates well with the pattern of the proteins missing from that of nonactin-treated flies. Nine new proteins also appear on the two-dimensional gels of the extracts from the nonactin-treated flies. Apparently, these nine proteins are precursors of the mature mitochondrial forms. These particular data support the concept that processing of many of the cytoplasmically synthesized mitochondrial proteins requires a specific membrane potential, and that some of these proteins are modified intramitochondrially. However, using [³⁵S]methionine incorporation techniques, not all labeled polypeptides disappear from mitochondria during such treatment. Feeding similarly radiolabeled flies with chloramphenicol, an inhibitor of mitochondrial protein synthesis, results in the disappearance of only one protein from the gel pattern with the concurrent appearance of a ‘new’ high-molecular-weight polypeptide. Collectively, these data show that a specific group of [³⁵S]methionine-labeled mitochondrial proteins can be identified by selective inhibition of mitochondrial function in whole cell protein maps of adult D. melanogaster.