DNA-Binding Magnetic Nanoreactor Beads for Digital PCR Analysis.

Digital PCR (dPCR) is based on the separation of target amplification reactions into many compartments with randomly distributed template molecules. Here, we present a novel digital PCR format based on DNA binding magnetic nanoreactor beads (mNRBs). Our approach relies on the binding of all nucleic acids present in a sample to the mNRBs, which both provide a high-capacity binding matrix for capturing nucleic acids from a sample and define the space available for PCR amplification by the internal volume of their hydrogel core.

Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy.

Membrane-shaping proteins characterized by reticulon homology domains play an important part in the dynamic remodelling of the endoplasmic reticulum (ER). An example of such a protein is FAM134B, which can bind LC3 proteins and mediate the degradation of ER sheets through selective autophagy (ER-phagy). Mutations in FAM134B result in a neurodegenerative disorder in humans that mainly affects sensory and autonomic neurons.

Disulfide cross-linking influences symbiotic activities of nodule peptide NCR247.

Interactions of rhizobia with legumes establish the chronic intracellular infection that underlies symbiosis. Within nodules of inverted repeat-lacking clade (IRLC) legumes, rhizobia differentiate into nitrogen-fixing bacteroids. This terminal differentiation is driven by host nodule-specific cysteine-rich (NCR) peptides that orchestrate the adaptation of free-living bacteria into intracellular residents.

Antibiotica research in Jena from penicillin and nourseothricin to interferon.

Milestones of antibiotics research and biotechnology in Jena/Thuringia are: 1938--Hans Knöll established a strain collection of microorganisms; 1942--production of penicillin on laboratory scale by Hans Knöll; since 1945--development of industrial production processes for penicillin and streptomycin; 1952--production of BCG-vaccine; since 1956--development of biotechnical processes in the Institute of Microbiology and Experimental Therapy for actinomycin C, oxytetracyclin, erythromycin, paromomycin, turimycin, griseofulvin, nystatin, and nourseothricin, and in the 1980s for streptokinase, staphylokinase, and interferons. After the German unification the Hans-Knöll-Institute for Natural Products Research was founded.