Studies on the quaternary structure of the first enzyme for histidine biosynthesis

Resumen Se han realizado estudios de asociación-disociación por filtración en gel con el primer enzima de la biosíntesis de histidina enEscherichia coli, en presencia de sustratos y ligandos. Se observa una interconversión reversible entre las formas dímero, tetrámero y exámero, y una agregación irreversible de orden superior.     

Neue lokalanästhetisch wirksame basische Cycloalkylester von substituierten Carbanilsäuren

Summary Highly active local anaesthetics from the group of basic substituted cyclohexylesters of 2-chloro-, 2, 6-dichloro-, 2-chloro-6-methyl-, 2-methyl-, 2, 6-dimethyl-and 2,4,6-trimethylcarbanilic acid were developed. The substances were tested for local anaesthetic activity in surface anaesthesia.     

Origin of AIDS: contaminated polio vaccine theory refuted

Despite strong evidence to the contrary, speculation continues that the AIDS virus, human immunodeficiency virus type 1 (HIV-1), may have crossed into humans as a result of contamination of the oral polio vaccine (OPV). This 'OPV/AIDS theory' claims that chimpanzees from the vicinity of Stanleyville--now Kisangani in the Democratic Republic of Congo--were the source of a simian immunodeficiency virus (SIVcpz) that was transmitted to humans when chimpanzee tissues were allegedly used in the preparation of OPV. Here we show that SIVcpz is indeed endemic in wild chimpanzees of this region but that the circulating virus is phylogenetically distinct from all strains of HIV-1, providing direct evidence that these chimpanzees were not the source of the human AIDS pandemic.     

Metabolic network analysis of the causes and evolution of enzyme dispensability in yeast

Under laboratory conditions 80% of yeast genes seem not to be essential for viability. This raises the question of what the mechanistic basis for dispensability is, and whether it is the result of selection for buffering or an incidental side product. Here we analyse these issues using an in silico flux model of the yeast metabolic network. The model correctly predicts the knockout fitness effects in 88% of the genes studied and in vivo fluxes. Dispensable genes might be important, but under conditions not yet examined in the laboratory. Our model indicates that this is the dominant explanation for apparent dispensability, accounting for 37-68% of dispensable genes, whereas 15-28% of them are compensated by a duplicate, and only 4-17% are buffered by metabolic network flux reorganization. For over one-half of those not important under nutrient-rich conditions, we can predict conditions when they will be important. As expected, such condition-specific genes have a more restricted phylogenetic distribution. Gene duplicates catalysing the same reaction are not more common for indispensable reactions, suggesting that the reason for their retention is not to provide compensation. Instead their presence is better explained by selection for high enzymatic flux.