Effects of protein content and rumen-undegradable to rumen-degradable protein ratio in finely ground calf starters on growth performance, ruminal and blood parameters, and urinary purine derivatives.

This study investigated the effects of feeding finely ground starter diets containing either 18 or 22% crude protein (CP) content [dry matter (DM) basis] and high or low ratios of rumen-undegradable protein to rumen-degradable protein (RUP:RDP) on growth performance, nutrient digestibility, ruminal fermentation, blood metabolites, and urinary purine derivatives in dairy calves. A total of 48 three-day-old female Holstein dairy calves with 40.2 ± 2.5 kg of initial body weight (BW) were randomly assigned in a complete randomized block design to a 2 × 2 factorial arrangement of treatments (12 calves/treatment). Treatments were as follows: (1) finely ground starter diet (mean particle size = 0.69 mm) with 18% CP and low RUP:RDP ratio [low ratio (LR) = 26:74; 18CP-LR]; (2) finely ground starter diet with 18% CP and high RUP:RDP ratio [high ratio (HR) = 35:65; 18CP-HR]; (3) finely ground starter diet with 22% CP and low RUP:RDP ratio (22CP-LR); (4) finely ground starter diet with 22% CP and high RUP:RDP ratio (22CP-HR) on DM bases. Blocking was based on the day of treatment assignment, and treatments were randomly assigned within each block. Calves received 4 L of milk daily from d 3 to 10, 7 L/d from d 11 to 40, 4 L/d from d 41 to 49, and 2.5 L/d from d 50 to 53, and then all calves were weaned but remained in the experiment until d 83 of age. The results showed that overall average daily gain (ADG), weaning BW, and feed efficiency (FE) were greater in 22% CP treatments than in 18% CP. Increasing the starter CP content from 18 to 22% of DM did not influence overall starter feed intake, milk intake, total dry matter intake (DMI), postweaning ADG, and FE of calves. No effect of RUP:RDP ratio was observed for starter feed intake, milk intake, total DMI, preweaning ADG, FE, and grams of CP per megacalorie of metabolizable energy. The RUP intake and postweaning ADG were greater for calves fed the HR diets than for those fed the LR diets. The digestibility of neutral detergent fiber was greater, and the digestibility of OM tended to be greater, and the ruminal concentrations of total short-chain fatty acids (SCFA), acetate proportion, and acetate-to-propionate ratio were greater in 22% CP than in 18% CP. A 2-way interaction between starter protein content and time was observed for total ruminal SCFA, acetate proportion, and acetate-to-propionate ratio, indicating that starter CP concentration had more effect on ruminal parameters. Preweaning urinary purine derivatives, preweaning microbial protein synthesis, and postweaning urinary nitrogen were greater for calves fed the 22CP diets than for those fed the 18CP diets but were not affected by the different RUP:RDP ratios. The concentrations of blood glucose and insulin were greater in 22% CP than in 18% CP diets. The blood insulin concentration was greater when calves received the HR diets compared with the LR diets. Therefore, we conclude that greater starter protein content can have beneficial effects on growth performance, probably through increased microbial protein synthesized and preweaning blood insulin concentration; however, a greater RUP:RDP ratio showed marginal effects on growth performance during the postweaning period.

Soybean oil supplementation and starter protein content: Effects on growth performance, digestibility, ruminal fermentation, and urinary purine derivatives of Holstein dairy calves.

This study investigated the effects of feeding dairy calves starter diets containing 19% or 22% crude protein (CP) content on a dry matter basis and either supplemented or not with soybean oil (SBO, 0 vs. 3%, dry matter basis) on growth performance, digestibility, urinary nitrogen, and purine derivatives (PD) excretion. A total of 48 female Holstein dairy calves (mean 39.8 kg of body weight) were randomly distributed to experimental diets in a 2 × 2 factorial arrangement of treatments. The 4 dietary treatments were (1) starter diet without SBO supplement and 19% CP (NSBO-19CP), (2) starter diet without SBO supplement and 22% CP (NSBO-22CP), (3) starter diet with 3% SBO and 19% CP (SBO-19CP), and (4) starter diet with 3% SBO and 22% CP (SBO-22CP). Milk feeding value was similarly based on a constant protocol across experimental treatments and calves had ad libitum access to water and starter diets throughout the study. All calves were weaned on d 63 of age and remained in the study until d 83 of age. Calves supplemented with SBO had lower starter feed intake and average daily gain (ADG) and lower feed efficiency (FE) but had a higher fecal score indicating a higher likelihood of diarrhea occurrence compared with unsupplemented calves. Wither heights, digestibilities of organic matter, CP, and neutral detergent fiber were decreased, and ruminal volatile fatty acids tended to be reduced, and the molar proportion of ruminal butyrate (preweaning) and acetate (postweaning) reduced by supplemental SBO. The urinary allantoin and total PD excretion were reduced; however, urinary nitrogen excretion was increased when calves were supplemented with SBO. The CP amount did not affect starter feed intake, FE, or diarrhea occurrence rate, whereas the 22CP diets increased neutral detergent fiber digestibility, improved ADG (tendency), and increased allantoin and urinary PD excretion compared with the 19CP diets. The starter feed intake, ADG, FE, diarrhea occurrence rate, nutrient digestibility, and ruminal fermentation were not affected by the interaction between starter SBO and CP level; however, hip height and total PD in calves that received the SBO-22CP diets were higher than those fed the SBO-19CP diets. In conclusion, based on our experimental conditions, supplemental SBO could not be recommended for dairy calves. Furthermore, our findings indicate that SBO has negative effects on performance more attributed to reducing starter intake, digestibility, and ruminal volatile fatty acid concentration rather than because of a limitation of starter metabolizable protein supply and intestinal amino acid availability. Therefore, our results indicate that feeding the higher starter CP content is not a viable strategy to compensate for the negative effects of SBO supplementation on the growth performance of dairy calves.

Application of merged spectroscopic data combined with chemometric analysis for resolution of hemoglobin intermediates during chemical unfolding.

Using tetradecyltrimethylammonium bromide (TTAB) as a surfactant denaturant, and augmentation of different spectroscopic data, helped to detect the intermediates of hemoglobin (Hb) during unfolding process. UV-vis, fluorescence, and circular dichroism spectroscopy were used simultaneously to monitor different aspects of hemoglobin species from the tertiary or secondary structure points of view. Application of the multivariate curve resolution-alternating least square (MCR-ALS), using the initial estimates of spectral profiles and appropriate constraints on different parts of augmented spectroscopic data, showed good efficiency for characterization of intermediates during Hb unfolding. These results indicated the existence of five protein species, including three intermediate-like compounds in this process. The unfolding pathway in the presence of TTAB included conversion of oxyhemoglobin into deoxyhemoglobin, and then ferrylhemoglobin, ferrihemoglobin or aquamethemoglobin, which finally transformed into hemichrome. This is the first application of chemometric analysis on the merged spectroscopic data related to chemical denaturation of a protein. These types of analysis in multisubunit proteins not only increase the domain of information, but also can reduce the ambiguities of the obtained results.

Heme degradation upon production of endogenous hydrogen peroxide via interaction of hemoglobin with sodium dodecyl sulfate.

In this study the hemoglobin heme degradation upon interaction with sodium dodecyl sulfate (SDS) was investigated using UV-vis and fluorescence spectroscopy, multivariate curve resolution analysis, and chemiluminescence method. Our results showed that heme degradation occurred during interaction of hemoglobin with SDS producing three fluorescent components. We showed that the hydrogen peroxide, produced during this interaction, caused heme degradation. In addition, the endogenous hydrogen peroxide was more effective in hemoglobin heme degradation compared to exogenously added hydrogen peroxide. The endogenous form of hydrogen peroxide altered oxyHb to aquamethemoglobin and hemichrome at low concentration. In contrast, the exogenous hydrogen peroxide lacked this ability under same conditions.