Cartographie de restriction comparée de la séquence d''ADN hautement répétée coupée par Bam HI chez Papio papio et P. cynocephalus

Highly repeated DNA sequences from two baboon species (Papio papio and P. cynocephalus) have been compared using restriction endonucleases. The two species share a 343 base pairs tandemly repeated DNA, that is cut once by Bam HI. Papio cynocephalus differs from P. papio by loss of an EcoRI star site in the repeated sequence.     

High‐Performance Li–Se Battery Enabled via a One‐Piece Cathode Design

A high‐performance Li–Se battery is demonstrated by adopting a novel Se cathode design. The Se cathode is a one‐piece body combined with a Se deposited current collector and a solid polymer electrolyte (SPE). In the preparation of the Se cathode, Se is electrodeposited on Ni‐foam, and the pores are filled with SPE layers. Through this electrodeposition, the cathode is easily fabricated, and charge transports are facile. The use of the SPE layer offers a durable Se electrode, enhancing ion pathways, securing safety, and suppressing undesirable electrochemical reactions. Li–Se batteries assembled with the one‐piece Se cathode and Li‐metal anode, without using conductive carbon, polymer binder, and separator, exhibit ultrastable performance with a low capacity decay of 0.001% per cycle at 1 C over 3000 cycles. The rational design of a one‐piece electrode may hold great promise for the future development of energy storage devices with facile fabrication process and long‐term stability.     

Production of Polysaccharide from Starch and Identification of Constituent Sugars of the Preparation

A bacterium which belongs to Achromobacter sp. was isolated and named as Achromobacter mucosum nov. sp. Starch and dextrin were essential carbon sources to produce a polysaccharide effectively by the bacterium. Maltotriose was as effective as starch for the production of the polysaccharide, and glucose, maltose, isomaltose and panose were little effective. This indicates that the bacterium requires a definite configuration of carbon source to produce the polysaccharide effectively. The dry powder of the polysaccharide was prepared from 10 liters of broth in the yield of 34.9 g. Glucose, galactose, mannose and uronic acid were confirmed as the constituent sugars of the polysaccharide and it was most probable that the uronic acid was d-glucuronic acid.     

Molecular Determinants that Regulate Plasma Membrane Association of HIV-1 Gag

Human immunodeficiency virus type 1 assembly is a multistep process that occurs at the plasma membrane (PM). Targeting and binding of Gag to the PM are the first steps in this assembly process and are mediated by the matrix domain of Gag. This review highlights our current knowledge on viral and cellular determinants that affect specific interactions between Gag and the PM. We will discuss potential mechanisms by which the matrix domain might integrate three regulatory components, myristate, phosphatidylinositol-(4,5)-bisphosphate, and RNA, to ensure that human immunodeficiency virus type 1 assembly occurs at the PM.     

Recognition and cooperation between the ATP-dependent RNA helicase RhlB and ribonuclease RNase E

The Escherichia coli protein RhlB is an ATP-dependent motor that unfolds structured RNA for destruction by partner ribonucleases. In E. coli, and probably many other related gamma-proteobacteria, RhlB associates with the essential endoribonuclease RNase E as part of the multi-enzyme RNA degradosome assembly. The interaction with RNase E boosts RhlB's ATPase activity by an order of magnitude. Here, we examine the origins and implications of this effect. The location of the interaction sites on both RNase E and RhlB are refined and analysed using limited protease digestion, domain cross-linking and homology modelling. These data indicate that RhlB's carboxy-terminal RecA-like domain engages a segment of RNase E that is no greater than 64 residues. The interaction between RhlB and RNase E has two important consequences: first, the interaction itself stimulates the unwinding and ATPase activities of RhlB; second, RhlB gains proximity to two RNA-binding sites on RNase E, with which it cooperates to unwind RNA. Our homology model identifies a pattern of residues in RhlB that may be key for recognition of RNase E and which may communicate the activating effects. Our data also suggest that the association with RNase E may partially repress the RNA-binding activity of RhlB. This repression may in fact permit the interplay of the helicase and adjacent RNA binding segments as part of a process that steers substrates to either processing or destruction, depending on context, within the RNA degradosome assembly.     

High‐Performance Large‐Area Organic Solar Cells Enabled by Sequential Bilayer Processing via Nonhalogenated Solvents

While the performance of laboratory‐scale organic solar cells (OSCs) continues to grow over 13%, the development of high‐efficiency large area OSCs still lags. One big challenge is that the formation of bulk heterojunction morphology is an extremely complicated process and the formed morphology is also a highly delicate balance involving many parameters such as domain size, purity, miscibility, etc. The morphology control becomes much more challenging when the device area is scaled up. In this work, a highly efficient (12.9%) nonfullerene organic solar cell processed using a sequential bilayer deposition method from nonhalogenated solvents, is reported. Using this bilayer processing method, the organic solar cells can be scaled up to a larger area (1 cm²) while maintaining a high performance of 11.4% using doctor‐blade‐coating technique. Moreover, as the acceptor is hidden behind the polymer donor, the possibility of degradation by sunlight is lessened. Thus, improved photostability is observed in the bilayer structure device when compared with the bulk heterojunction device. This method offers a truly compatible processing technique for printing large‐area OSC modules.