Six isonitrogenous (390 g kg )1 ) and isoenergetic (16.2 kJ g )1 ) diets with varying carbohydrate : lipid (CHO : L) ratios (202.5-1.74), were fed to triplicate groups of 25 fish in indoor recirculation system. Over 8-week-growth trial, best weight gain (WG), specific growth rate, feed conversion ratio, protein efficiency ratio and protein production value (P < 0.05) were observed in fish-fed diets with CHO : L ratio of 7.5. Fish fed either the lowest (1.7) or highest (202.5) CHO : L ratio tended to produce lower (P < 0.05) growth and feed conversion efficiencies. The values of viscerosomatic index, hepatosomatic index and intraperitoneal fat ratio increased as dietary CHO : L ratios decreased. There were no significant differences in whole body and liver crude protein among dietary treatments. Whole body and liver lipid increased as CHO : L ratios decreased. Plasma cholesterol and triacylglyceride levels increased linearly as dietary CHO : L ratios decreased. Activities of glucokinase and pyruvate kinase were stimulated by elevated levels of dietary carbohydrate; however, activities of lipase (LPS) and alkaline phosphatase were stimulated by elevated levels of dietary lipid. Based on a second-order polynomial regression analysis of WG against dietary carbohydrate and lipid levels, 275 g kg )1 of carbohydrate and 59 g kg )1 of lipid, corresponding to a CHO : L ratio of 4.7, in a diet holding 390 g kg )1 of crude protein and 16.3 kJ g )1 of gross energy, proved to be optimal for grass carp. These results indicated that utilization of dietary lipid and carbohydrate was moderate in grass carp, but the fish were a little more capable of utilizing lipid compared with carbohydrate. KEY WORDS
Two, 8‐week feeding trials were conducted to compare protein‐sparing capability of dietary lipid in herbivorous grass carp (Ctenopharyngodon idella) and omnivorous tilapia (Oreochomis niloticus × O. aureus). Utilizing a 2 × 3 factorial design, experimental diets containing two levels of crude protein (380 and 250 g kg−1) and three levels of lipid (0, 40 and 100 g kg−1) were formulated for use in both feeding trials. Growth performances showed better response of both fish fed 380 g kg−1 protein diet than those fed 250 g kg−1 protein diet. Despite the dietary protein level, weight gain (WG), specific growth ratio (SGR), feed conversion ratio (FCR) and protein efficiency ratio were much higher (P < 0.05) for grass carp fed 40 g kg−1 lipid diet than those fed 100 g kg−1 lipid diet; however, there were no significant differences in tilapia fed the two diets. The feed intake of grass carp fed lipid‐free diet was the lowest, but it tended to decrease with increase in dietary lipids in tilapia. Lipid retention (LR) was negatively correlated with dietary lipid concentration of both fish. Viscerosomatic index (VSI), hepatosomatic index (HSI), intraperitoneal fat ratio (IPF) and whole‐body and liver lipid content positively correlated with dietary lipid concentration of both fish. Plasma parameters and liver enzymes activities were also positively correlated with dietary lipid concentration of both fish. Liver lipid contents were higher and enzymes activities were lower in grass carp when compared with tilapia. These data suggested that there was no evidence of a protein‐sparing effect of dietary lipids in grass carp. Tilapia has relatively higher capacity to endure high dietary lipid level compared to grass carp.
Two experiments were conducted to evaluate the effect of lowering crude protein level and fish-meal inclusion rate by using commercially available synthetic amino acid supplements in practical diets on the growth performance of Litopenaeus vannamei. In experiment 1, three diets were formulated to assess whether 50% of fish meal could be replaced by soybean meal with synthetic amino acid supplementation. Diet 1 was formulated as the normal control with 20% fish meal and 36% crude protein; diet 2 was the negative control with 34% crude protein and half of the fish meal was replaced with soybean meal; and diet 3 was similar to diet 2 but was supplemented with amino acids to ensure the level of lysine, methionine plus cystine, and threonine similar to that in the diet 1. After a 70-day feeding trial, weight gain and specific growth rate of shrimps fed diet 2 were significantly lower than those fed diet 3, and numerically lower than those fed diet 1. Feed intake of shrimps fed diet 3 was significantly higher than those fed diets 1 and 2. There were no significant differences in feed conversion ratio among shrimps fed different diets. In experiment 2, four diets were prepared with diet 1 as the normal control with 41.26% crude protein, diets 2-4 were formulated to contain 39.81, 38.40, and 35.52% of crude protein with synthetic amino acids were added to simulate the amino acid levels of the diet 1. After a 70-day feeding trial, it was found that reducing dietary crude protein from 41.26 to 35.52% did not affect weight gain or feed conversion ratio. The survival of crude protein 35.52% treatment was significantly lower than other treatments. No difference was observed in body protein, lipid composition, and apparent digestibility coefficient among dietary treatments. Results of this study suggested that dietary crude protein could be reduced from 41.26 to 35.52% in the diets of L. vannamei as long as synthetic amino acids were supplemented.
An 8‐week feeding trial was conducted to determine the threonine requirement of juvenile Pacific white shrimp Litopenaeus vannamei (Boone) in low‐salinity water (0.50–1.50 g L−1). Diets 1–6 were formulated to contain 360 g kg−1 crude protein with fish meal, wheat gluten and pre‐coated crystalline amino acids with six graded levels of l‐threonine (9.9–19.0 g kg−1 dry diet). Diet 7, which was served as a reference, contained only intact proteins (fish meal and wheat gluten). Each diet was randomly assigned to triplicate groups of 30 shrimps (0.48±0.01 g), each four times daily. Shrimps fed the reference diet had similar growth performance and feed utilization efficiency compared with shrimps fed the diets containing 13.3 g kg−1 or higher threonine. Maximum specific growth rate (SGR) and protein efficiency ratio were obtained at 14.6 g kg−1 dietary threonine, and increasing threonine beyond this level did not result in a better performance. Body compositions, triacyglycerol and total protein concentrations in haemolymph were significantly affected by the threonine level; however, the threonine contents in muscle, aspartate aminotransferase and alanine aminotransferase activities in haemolymph were not influenced by the dietary threonine levels. Broken‐line regression analysis on SGR indicated that optimal dietary threonine requirement for L. vannamei was 13.6 g kg−1 dry diet (37.8 g kg−1 dietary protein).
This study was conducted to investigate the effects of replacing inorganic trace minerals ( ITM ) with organic trace minerals ( OTM ; complexed glycinates) on reproductive performance, blood profiles, and antioxidant status in broiler breeders. A total of 648, 23-week-old healthy broiler breeders (ZhenNing), with similar body weight (1.40 ± 0.002 kg), were randomly divided into 4 groups with 6 replicates in each group (27 hens/replicate) and fed the respective experimental diets for 14 wk (including 2 wk for adaptation). The experimental treatments consisted of T1: Cont., commercially recommended levels of ITM (Cu, Zn, Fe, and Mn sulfates); T2: Mix, half trace minerals ( TM ) were provided from ITM and half from OTM (glycinates); T3: M-OTM, TM were provided from glycinates and reduced to 70% of T1; T4: L-OTM, TM were provided from glycinates and reduced to 50% of T1. The results showed that commercial level of inorganic trace minerals replaced by low-dose complexed glycinates (T3 and T4) exhibited no significant effects on laying performance, 50% ITM replaced by complexed glycinates (T2) numerically improved laying rate by 1.23% than cont. treatment (T1). Broiler breeders fed complexed glycinates tended to produce more qualified eggs ( P = 0.05) in T3, with better yolk color ( P < 0.01) and eggshell thickness ( P = 0.05) in T2 treatment. Replacement of low-dose complexed glycinates reduced fertilization rate ( P < 0.01), while it did not affect hatchability. There were no significant differences in serum reproductive hormones such as estrogen and progesterone among the treatments. Serum total protein, albumin, and phosphorus were increased respectively with the replacement of ITM by low-dose OTM from complexed glycinates ( P < 0.05). Total liver antioxidant capacity in M-OTM and L-OTM treatment was higher than that of Cont. and Mix treatments ( P < 0.01). In conclusion, replacement of high levels of ITM by lower levels of OTM in the form of complexed glycinates is beneficial for egg quality and liver antioxidant status in broiler breeders during the peak laying period.
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