Low protein

About: Low protein is a research topic. Over the lifetime, 8139 publications have been published within this topic receiving 213225 citations.

Effect of protein A on staphylococcal opsonization.

Abstract: To study the effect of wall protein A on bacterial opsonization, phagocytosis of 10 strains of Staphylococcus aureus with high and low protein A contents was measured. Those strains that contained the highest concentrations of protein A were phagocytized by human neutrophils at a slower rate than strains with little or no protein A when normal human serum and purified immunoglobulin G (IgG) were used as opsonic sources. When IgG-deficient serum was used as an source, however, protein A-rich strains were phagocytized more rapidly than protein A-deficient strains. Extracellular (purified) protein A decrease the opsonic activity of all sera tested including IgG-deficient serum. It is proposed that when IgG is not present in the opsonic medium, cell wall protein A is capable of activating complement at the bacterial surface and thereby opsonization is promoted.

Energy utilization of low-protein diets in growing pigs.

Abstract: Three trials were conducted to measure the effects of reducing the dietary CP content on digestive and metabolic utilization of N and energy in growing pigs. Sixty barrows weighing about 65 kg were used. In Trial 1, four semisynthetic diets with CP content decreasing from 18.9 to 12.3% were formulated. In Trials 2 and 3, two diets with 17.4 and 13.9% CP were formulated using conventional ingredients. In the three trials, diets were supplemented with variable amounts of industrial AA in order to maintain a constant standardized digestible lysine/NE ratio (0.76 g/MJ) and ratios between essential AA relative to lysine of at least 60, 65, 20, 60, and 70% for methionine + cystine, threonine, tryptophan, isoleucine, and valine, respectively. In Trials 1 and 2, feed was given in four meals per day, whereas, in Trial 3, two feeding frequencies (two and seven meals per day) were compared. Five or six N and energy balance (indirect calorimetry) measurements were conducted for each treatment, and components of heat production were estimated. Results of Trial 3 showed no effect of meal frequency on either N or energy utilization. Reduction of dietary CP content had no effect on N retention or animal performance but markedly decreased N excretion (-40% in Trials 2 and 3, and -58% in Trial 1). In the three trials, the lower N excretion with low-CP diets was accompanied by a reduction in urinary energy loss equivalent to 3.5 kJ/g of decrease in protein intake. Data of the three trials indicated that heat production was lower when CP was reduced (-7 kJ/g decrease in protein intake). This lower heat production was attributed to a reduction of the thermic effect of feed, whereas heat production associated with physical activity and maintenance were not affected. Reduction of dietary CP was associated with higher energy gain, mainly as fat. But, this effect was no longer significant when data were adjusted for similar NE intakes. These results confirm the possibility of limiting N excretion, while maintaining a high level of performance, by reducing CP level in the feed with adequate AA supplementation. This study also confirms the superiority of the NE system (in comparison with DE or ME systems) for predicting performance and energy gain of pigs and controlling carcass adiposity, especially in situations of feeds with variable CP contents.

Signal sequences directing cotranslational translocation expand the range of proteins amenable to phage display.

Abstract: Even proteins that fold well in bacteria are frequently displayed poorly on filamentous phages. Low protein presentation on phage might be caused by premature cytoplasmic folding, leading to inefficient translocation into the periplasm. As translocation is an intermediate step in phage assembly, we tested the display levels of a range of proteins using different translocation pathways by employing different signal sequences. Directing proteins to the cotranslational signal recognition particle (SRP) translocation pathway resulted in much higher display levels than directing them to the conventional post-translational Sec translocation pathway. For example, the display levels of designed ankyrin-repeat proteins (DARPins) were improved up to 700-fold by simply exchanging Sec- for SRP-dependent signal sequences. In model experiments this exchange of signal sequences improved phage display from tenfold enrichment to >1,000-fold enrichment per phage display selection round. We named this method 'SRP phage display' and envision broad applicability, especially when displaying cDNA libraries or very stable and fast-folding proteins from libraries of alternative scaffolds.