Evaluation of electronic pheromone trap capture conditions for Ips sexdentatus with climatic and temporal factors.

Controlling forest pests to maintain the sustainability of forests and ecosystem balance is one of the interests of modern forestry. In the evaluation of damage risks associated with forest pests, pheromone traps attract attention by providing early warnings. With the development of these traps in line with modern technology, more reliable data are obtained; these data are important in the identification and planning of pest management.

Peroxisomes: offshoots of the ER.

Peroxisomes are part of the ubiquitous set of eukaryotic organelles. They are small, single membrane bounded vesicles, specialized in the degradation of very-long-chain fatty acids and in synthesis of myelin lipids. Once considered inconspicuous, recent new insights in the formation and function of peroxisomes have revealed a much more subtle interplay between organelles that warrant a re-evaluation of the historical assignment of peroxisomes as being either autonomous or ER-derived.

Peroxisome formation and maintenance are dependent on the endoplasmic reticulum.

Looks can be deceiving. Although peroxisomes appear to be simple organelles, their formation and maintenance pose unique challenges for the cell. The birth of new peroxisomes starts at the endoplasmic reticulum (ER), which delivers lipids and membrane proteins.

Biochemically distinct vesicles from the endoplasmic reticulum fuse to form peroxisomes.

As a rule, organelles in eukaryotic cells can derive only from pre-existing organelles. Peroxisomes are unique because they acquire their lipids and membrane proteins from the endoplasmic reticulum (ER), whereas they import their matrix proteins directly from the cytosol. We have discovered that peroxisomes are formed via heterotypic fusion of at least two biochemically distinct preperoxisomal vesicle pools that arise from the ER.

Peroxisomal membrane proteins insert into the endoplasmic reticulum.

We show that a comprehensive set of 16 peroxisomal membrane proteins (PMPs) encompassing all types of membrane topologies first target to the endoplasmic reticulum (ER) in Saccharomyces cerevisiae. These PMPs insert into the ER membrane via the protein import complexes Sec61p and Get3p (for tail-anchored proteins). This trafficking pathway is representative for multiplying wild-type cells in which the peroxisome population needs to be maintained, as well as for mutant cells lacking peroxisomes in which new peroxisomes form after complementation with the wild-type version of the mutant gene.