Phykochronologische Untersuchungen in Assoziationen von Laminaria digitata (L.) Lamour. f. stenophylla (Kütz.) Harv. an der norwegischen Westküste

Zusammenfassung Die Natur der konzentrischen Zonen in den Stämmen von Laminarien ist lange Zeit umstritten gewesen. Nachdem aber im Jahre 1926 nachgewiesen wurde, daß das gesamte vegetative Wachstum bei den nordischen, regelmäßig blatterneuernden Laminarien periodisch und synchron in allen Teilen der Pflanzen erfolgt, war damit bewiesen, daß diese Zonen wirkliche Jahresringe darstellen, die im Zusammenhang mit dem jährlichen Blattwechsel stehen.Ebenso wie die Dendrochronologie die Jahresringe der Bäume als Grundlage für forstliche Untersuchungen über Bestockung, Alter, Produktions- und Verjüngungsverhältnisse im Waldbau benutzt, kann man aus den Jahresringen der nordischen Laminarien entsprechende Rückschlüsse ziehen.Bei der stetig steigenden Nutzbarmachung und Verwendung der Meeresalgen sind derartige Gesichtspunkte von aktuellem Interesse in der Algologie geworden.Vorliegende Arbeit ist ein Versuch, eine Bestandsanalyse in phykochronologischer Regie durchzuführen mit besonderer Berücksichtigung etwaiger Schwankungen in Assoziationen von Laminaria digitata f. stenophylla hinsichtlich Repopulation, Bestockung, Wachstumsverhältnissen und anderer damit verknüpfter biologischer Fragen.Die Untersuchung wurde in den Jahren 1955–1958 an der norwegischen Westküste vorgenommen.Es sei darauf hingewiesen, daß sowohl das vegetative Wachstum als auch die Repopulation bei der genannten Alge von Jahr zu Jahr innerhalb ausgedehnten Grenzen variieren kann und daß diese Pflanze eine nur kurze Lebensdauer hat. Exemplare von mehr als 6 Jahren wurde nicht angetroffen. Ihr Bestand wird deshalb recht rasch erneuert.Professor Dr. E. G. Pringsheim zum 80. Geburtstag gewidmet.     

The oxidative inactivation of plasminogen activator inhibitor type 1 results from a conformational change in the molecule and does not require the involvement of the P1' methionine.

Plasminogen activator inhibitor 1 (PAI-1) is sensitive to oxidative inactivation, and it has been suggested that specific oxidation of a methionine residue, Met347, situated in the P1' position of the reactive center may be the cause of the inactivation. To test this hypothesis we have purified and biochemically characterized mutant proteins of PAI-1 in which Met347 and either of two other methionines, Met266 or Met354, has been replaced with oxidation-resistant valine residues. The mutant proteins were found to be equally sensitive to oxidation as wild-type PAI-1, suggesting that a specific oxidation of the P1' Met347 is not responsible for the inactivation. When PAI-1 was oxidized, circular dichroism analysis revealed a rapid conformational change that correlated to the loss of inhibitory activity. The oxidation sensitivity of PAI-1 was enhanced dramatically in the presence of 0.001% sodium dodecyl sulfate, and the circular dichroism spectrum was significantly different from that of untreated PAI-1, suggesting that the increased sensitivity to oxidation may be caused by a conformational change in the inhibitor molecule. Taken together, our data suggest that the oxidative inactivation of PAI-1 is not caused by the specific oxidation of the P1' methionine but results from a conformational change in the protein structure.     

Notes on the genus Pteroceras (Orchidaceae)

A new name (Pteroceras semiteretifolium H. Æ. Peders.) and two new combinations (P. cladostachyum (Hook.f.) H. Æ. Peders., P. unguiculatum (Lindley) H. Æ. Peders.) are presented. The correct application of the name P. pallidum (Blume) Holttum is discussed.     

Evolution of structure and function of V-ATPases

Proton pumping ATPases/ATPsynthases are found in all groups of present-day organisms. The structure of V- and F-type ATPases/ATP synthases is very conserved throughout evolution. Sequence analysis shows that the V- and F-type ATPases evolved from the same enzyme already present in the last common ancestor of all known extant life forms. The catalytic and noncatalytic subunits found in the dissociable head groups of the V/F-type ATPases are paralogous subunits, i.e., these two types of subunits evolved from a common ancestral gene. The gene duplication giving rise to these two genes (i.e., encoding the catalytic and noncatalytic subunits) predates the time of the last common ancestor.Mapping of gene duplication events that occurred in the evolution of the proteolipid, the noncatalytic and the catalytic subunits, onto the tree of life leads to a prediction for the likely subunit structure of the encoded ATPases. A correlation between structure and function of V/F-ATPases has been established for present-day organisms. Implications resulting from this correlation for the bioenergetics operative in proto-eukaryotes and in the last common ancestor are presented. The similarities of the V/F-ATPase subunits to an ATPase-like protein that was implicated to play a role in flagellar assembly are evaluated.Different V-ATPase isoforms have been detected in some higher eukaryotes. These data are analyzed with respect to the possible function of the different isoforms (tissue specific, organelle specific) and with respect to the point in their evolution when these gene duplications giving rise to the isoforms had occurred, i.e., how far these isoforms are distributed.     

Inheritance of the group I rDNA intron in Tetrahymena pigmentosa

We have previously argued from phylogenetic sequence data that the group I intron in the rRNA genes of Tetrahymena was acquired by different Tetrahymena species at different times during evolution. We have now approached the question of intron mobility experimentally by crossing intron⁺ and intron^? strains looking for a strong polarity in the inheritance of the intron (intron homing). Based on the genetic analysis we find that the intron in T. pigmentosa is inherited as a neutral character and that intron⁺ and intron^? alleles segregate in a Mendelian fashion with no sign of intron homing. In an analysis of vegetatively growing cells containing intron⁺ and intron^? rDNA, initially in the same macronucleus, we similarly find no evidence of intron homing. During the course of this work, we observed to our surprise that progeny clones from some crosses contained three types of rDNA. One possible explanation is that T. pigmentosa has two rdn loci in contrast to the single locus found in T. thermophila. Some of the progeny clones from the genetic analysis were expanded for several hundred generations, and allelic assortment of the rDNA was demonstrated by subcloning analysis. © 1992 Wiley-Liss, Inc.