An engineered retroviral proteinase from myeloblastosis associated virus acquires pH dependence and substrate specificity of the HIV-1 proteinase

In an attempt to understand the structural reasons for differences in specificity and activity of proteinases from two retroviruses encoded by human immunodeficiency virus (HIV) and myeloblastosis associated virus (MAV), we mutated five key residues predicted to form part of the enzyme subsites S1, S2 and S3 in the substrate binding cleft of the wild-type MAV proteinase wMAV PR. These were changed to the residues occupying a similar or identical position in the HIV-1 enzyme. The resultant mutated MAV proteinase (mMAV PR) exhibits increased enzymatic activity, altered substrate specificity, a substantially changed pH activity profile and a higher pH stability close to that observed in the HIV-1 PR. This dramatic alteration of MAV PR activity achieved by site-directed mutagenesis suggests that we have identified the amino acid residues contributing substantially to the differences between MAV and HIV-1 proteinases

Low-Temperature Carbon Capture Using Aqueous Ammonia and Organic Solvents

Current postcombustion CO₂ capture technologies are energy intensive, require high-temperature heat sources, and dramatically increase the cost of power generation. In this work, we introduce a new carbon capture process requiring significantly lower temperatures and less energy, creating further impetus to reduce CO₂ emissions from power generation. In this process, high-purity CO₂ is generated through the addition of an organic solvent (acetone, dimethoxymethane, or acetaldehyde) to a CO₂ rich, aqueous ammonia/carbon dioxide solution under room-temperature and -pressure conditions. The organic solvent and CO₂-absorbing solution are then regenerated using low-temperature heat. When acetone, dimethoxymethane, or acetaldehyde was added at a concentration of 16.7% (v/v) to 2 M aqueous ammonium bicarbonate, 39.8, 48.6, or 86.5%, respectively, of the aqueous CO₂ species transformed into high-purity CO₂ gas over 3 h. Thermal energy and temperature requirements for recovering acetaldehyde, the best-performing organic solvent investigated, and the CO₂-absorbing solution were 1.39 MJ/kg of CO₂ generated and 68 °C, respectively, 75% less energy than the amount used in a pilot chilled ammonia process and a temperature 53 °C lower. Our findings exhibit the promise of economically viable carbon capture powered entirely by abundant low-temperature waste heat