Dietary l‐lysine requirement of fingerling stinging catfish,Heteropneustes fossilis (Bloch) for optimizing growth,feed conversion,protein and lysine deposition

Dietary lysine requirement of fingerling Heteropneustes fossilis (6.96 ± 0.05 g) was quantified by conducting 12‐week feeding trial in a flow‐through system at 28°C. Casein–gelatin based isonitrogenous (38% CP) and isocaloric (14.7 kJ g^?1 DE) amino acid test diets with six levels of dietary lysine (1.5%, 1.75%, 2.0%, 2.25%, 2.5%, 3.0% dry diet) were fed to apparent satiation in triplicates. Broken‐line and second‐degree polynomial regression analyses at 95% plateau of absolute weight gain (AWG; g fish^?1), feed conversion ratio (FCR), protein deposition (PD; g fish^?1) and lysine deposition (LD; g fish^?1) exhibited lysine requirement between 2.0% to 2.3% of the dry diet, corresponding to 5.3–6.1% protein.     

Dietary L‐tryptophan requirement of fingerling stinging catfish,Heteropneustes fossilis (Bloch)

To quantify dietary L‐tryptophan requirement of fingerling Heteropneustes fossilis (6.66 ± 0.08 g), casein–gelatin‐based isonitrogenous (38% CP) and isoenergetic (14.72 kJ g^?1 DE) purified diets with eight levels of L‐tryptophan (0.12%, 0.16%, 0.20%, 0.24%, 0.28%, 0.32%, 0.36%, 0.40% dry diet) were fed to triplicate groups of fish twice daily to apparent satiation for 12 weeks. Incremental levels of dietary tryptophan from 0.12 to 0.28% significantly (P < 0.05) improved absolute weight gain (AWG; 14.3–65.9 g fish^?1), feed conversion ratio (FCR; 5.9–1.5), protein retention efficiency (PRE; 6.2–32.2%), haemoglobin (Hb; 6.5 to 11.9 g dL^?1) and haematocrit (Hct; 23.5–33.8%). To determine the precise information on tryptophan requirement, data were subjected to broken‐line and second‐degree polynomial regression analysis. Broken‐line regression analysis reflected highest R² values for AWG g fish^?1 (0.999), PRE% (0.993), Hb g dL^?1 (0.995) and Hct% (0.993) compared with R² values obtained using second‐degree polynomial regression analysis of AWG g fish^?1(0.949), PRE% (0.890), Hb g dL^?1(0.969) and Hct% (0.943), indicating that data were better fit to broken‐line regression analysis. Hence, based on broken‐line regression analysis at 95% maximum response, tryptophan requirement of fingerling H. fossilis is recommended between 0.24% and 0.27% dry diet (0.63–0.71% protein).     

Dietary histidine requirement of fingerling Catla Catla (Hamilton) based on growth,protein gain,histidine gain,RNA/DNA ratio,haematological indices and carcass composition

To investigate the histidine requirement of fingerling Catla catla (3.65 ± 0.15 cm; 0.65 ± 0.36 g), six casein‐gelatin based diets (33% CP; 13.58 kJ g^?1 DE) containing graded levels of L‐histidine (0.25%, 0.39%, 0.53%, 0.67%, 0.83%, 0.96% of the dry diet) were fed near to satiation thrice a day for 12 weeks. Maximum absolute weight gain (AWG; 8.63 g fish^?1), protein gain (PG; 1.45 g fish^?1), histidine gain (HG, 48.19 mg fish^?1), RNA/DNA ratio (4.15), best feed conversion ratio (FCR; 1.31), highest haemoglobin (Hb, 9.61 g dL^?1), RBCs (2.84 × 10⁶ mm^?3) and haematocrit (Ht, 30.12%) were recorded in fish fed diet containing 0.67% histidine. However, broken‐line regression analysis of AWG, PG, HG, RNA/DNA ratio, FCR, Hb, Ht and RBCs against dietary histidine reflected the histidine requirement at 0.65%, 0.64%, 0.63%, 0.68%, 0.63%, 0.66%, 0.68% and 0.65% dry diet respectively. Carcass protein was found to improve significantly (P < 0.05) from 13.36% to 16.42% with the increase in dietary histidine from 0.25% to 0.67%. Based on regression analysis of AWG, PG, HG, RNA/DNA ratio, FCR, Hb, Ht and RBCs, it is recommended that the diet for fingerling catla should contain histidine in the range of 0.63–0.68% dry diet, equivalent to 1.91–2.06% of the dietary protein for optimum growth, feed utilization, blood profile and carcass composition.     

Growth,feed conversion and body composition of fingerling stinging catfish Heteropneustes fossilis (Bloch) fed varying levels of dietary l‐threonine

An 8‐week feeding trial was conducted to assess the effects of dietary l ‐threonine on growth, protein utilization, threonine retention efficiencies, nucleic acid indices and body composition of fingerling Heteropneustes fossilis (6.6 ± 0.1 g; 10.9 ± 0.2 cm). Casein–gelatin based isonitrogenous (38% crude protein; CP) and isocaloric (15.3 kJ g^?1 digestible energy; DE) amino acid test diets with six levels of dietary l ‐threonine (0.75%; 1.0%; 1.25%; 1.5%; 1.75%; 2.0% dry diet) were prepared and hand‐fed to quadruplicate groups of fingerling to apparent visual satiation twice daily. Weight gain (WG; 46.3 g fish^?1), feed conversion ratio (FCR; 1.98), protein utilization efficiency (PUE; 0.25), threonine retention efficiency (TRE; 0.69), lipid productive value (LPV; 0.45), body protein (18.2%) and RNA/DNA ratio (3.6) of fish fed graded levels of dietary threonine increased significantly (P < 0.05) up to 1.49% threonine of dry diet. To generate precise information, the WG, RNA/DNA and LPV data were subjected to broken‐line and quadratic regression analyses. The two models were superimposed and requirement was determined by establishing the point, where the quadratic curve first intersected the plateau of broken‐line. Based on the above mathematical analyses, optimum dietary threonine requirement of fingerling H. fossilis was estimated to range between 1.62% and 1.69% of the diet, corresponding to 4.26–4.44% protein.     

Dietary copper requirement of fingerling Channa punctatus (Bloch) based on growth,feed conversion,blood parameters and whole body copper concentration

A 12‐week feeding trial was conducted to estimate the dietary copper requirement of fingerling Channa punctatus. Six casein?gelatin‐based test diets (450 g kg^?1 crude protein; 18.81 kJ g^?1 gross energy) with graded levels of copper as copper sulphate (3.7, 4.7, 5.7, 6.7, 7.7 and 8.7 mg copper equivalent kg^?1 diet) were formulated and fed to triplicate groups of fish (7.25 ± 0.81 cm; 5.21 ± 0.27 g) near to satiation. Fish fed diet with 6.7 mg kg^?1 copper had highest absolute weight gain (AWG; 51.63 g fish^?1), protein efficiency ratio (PER; 1.42 g fish^?1), protein gain (PG; 8.34 g fish^?1), haemoglobin (Hb; 9.68 g dL^?1), haematocrit (Hct; 31.18%) and RBCs (3.24 × 10⁶ × mm^?3). Feed conversion ratio (FCR) was found to be best (1.57) at above level of dietary copper. Whole body copper concentration was found to increase with the increasing levels of dietary copper. Hepatic thiobarbituric acid‐reactive substances concentration was found to decrease with increasing dietary concentrations of copper up to 6.7 mg kg^?1 beyond which a reverse trend in this parameter was noted. Broken‐line regression analysis of AWG, FCR and PG concentrations against varying levels of dietary copper yielded the requirement in the range of 6.66–6.78 mg kg^?1. Data generated during this study would be useful in formulating copper‐balanced commercial feeds for the intensive culture of this fish.     

Dietary leucine requirement of Juvenile Nile tilapia,Oreochromis niloticus

An 8‐week feeding trial was conducted to evaluate the effects of dietary leucine on growth performance, feed utilization, body composition and non‐specific immune responses of juvenile Nile tilapia. Five isonitrogenous and isoenergetic diets were formulated to contain graded levels of L‐leucine (5.3, 8.1, 10.9, 13.2, 15.6 and 18.1 g kg^?1 diet, respectively) from dietary ingredients and crystalline L‐leucine. Each diet was randomly assigned to triplicate groups of 20 juvenile fish (1.94 ± 0.01 g) three times daily to apparent satiation. Results showed that the weight gain (WG) and specific growth rate (SGR) increased as dietary leucine concentrations increased from 5.3 to 13.2 g kg^?1 and then decreased slightly with further increase in dietary leucine concentrations. Quadratic regression analysis (y = ?522.6x² + 1304.x + 132.6, R² = 0.684) on weight gain against dietary leucine levels indicated that the optimal dietary leucine requirement was estimated to be 12.5 g kg^?1 diet (corresponding to 43.1 g kg^?1 of dietary protein). Leucine supplementation had no impact on the survival and body composition of tilapia. Serum lysozyme activity of fish fed diet containing 13.2 g kg^?1 leucine significantly increased compared to fish fed diet containing 5.3 g kg^?1. Serum superoxide dismutase activity and immunoglobulin M (IgM) concentration were not significantly affected by dietary leucine supplementation.     

Dietary histidine requirement of Singhi,Heteropneustes fossilis fry (Bloch)

Amino acids are vital for all living organisms including fish and histidine is an essential amino acid for fish. In view of this, dietary histidine requirement of fry Heteropneustes fossilis was determined by feeding casein–gelatin‐based isonitrogenous (430 g kg^?1 CP) and isocaloric (17.9 MJ kg^?1 GE; 15.5 MJ kg^?1 DE) amino acid test diets (10 to 20 g histidine kg^?1 dry diet) to quadruplicate groups of randomly assigned fish to apparent satiety for 12 weeks. Maximum absolute weight gain (AWG; 44 g fish^?1), protein retention efficiency (PRE; 20%), protein efficiency ratio (PER; 1.04), haemoglobin (Hb; 11.24 g dL^?1), haematocrit (Hct; 35.11%), red blood count (RBCs; 2.98 × 10⁹ mL^?1) and lowest erythrocyte sedimentation rate (ESR; 1.92 mm h^?1) were obtained at 16 g histidine kg^?1 dry diet. The 95% maximum quadratic response of above data exhibited the requirement to be at 15.2, 15.1, 15.6 and 15.5 g histidine kg^?1 diet. As histidine is found in higher concentration in haemoglobin, requirement obtained for Hct% and Hb is 4% greater than that required for maximizing weight gain and protein retention. Based on these results, dietary histidine requirement of H. fossilis fry is recommended between 15.1 and 15.6 g kg^?1, corresponding to 35.1–36.3 g kg^?1 protein.     

Evaluation of feeding rate based on growth,feed conversion,protein gain and carcass quality of fingerling Indian major carp,Catla catla (Hamilton)

The effects of feeding rates on growth, feed conversion, protein deposition and carcass quality of fingerling Catla catla (3.61 ± 0.03 cm; 0.71 ± 0.04 g) were worked out by conducting a 16‐week feeding trial. Fingerlings were fed with a casein‐gelatin‐based purified diet (40% crude protein CP; 14.95 MJ kg^?1 digestible energy; DE) at 1%, 2%, 3%, 4%, 5%, 6% and 7% body weight per day. The absolute weight gain (AWG; 10.50 g fish^?1) and feed conversion ratio (FCR; 1.41) were highest at the feeding rate of 5% body weight per day. However, protein gain (PG; 0.36 g fish^?1) and carcass protein content attained the maximum values at 4% BW day^?1. Quadratic regression analyses of AWG g fish^?1 and PG g fish^?1 at 95% maximum response indicated that these parameters attained the best values at 4.19% and 3.81% BW day^?1. On the basis of the above results it is recommended that the feeding rate in the range of 3.81–4.19% BW day^?1 with a P:E ratio of 26.69–27.74 mg protein MJ^?1 DE is optimum for maximum growth, efficient feed conversion and best carcass quality in fingerling C. catla.     

Dietary arginine requirement of Heteropneustes fossilis fry (Bloch) based on growth,nutrient retention and haematological parameters

Dietary arginine requirement of Heteropneustes fossilis fry (3.0 ± 0.5 cm; 5.1 ± 0.3 g) was determined by feeding casein‐gelatin‐based isonitrogenous (400 g kg^?1 crude protein) and isocaloric (17.97 kJ g^?1) amino acid test diets containing graded levels of l ‐arginine (15, 17, 19, 21, 23 and 25 g kg^?1 dry diet) for 12 weeks. Maximum absolute weight gain (AWG) (44.4), best feed conversion ratio (FCR) (1.22), highest protein retention efficiency (PRE%) (41%), energy retention efficiency (ERE%) (75%), best condition factor, hepatosomatic index and viscerosomatic index were noted at 21 g kg^?1 arginine of the dry diet. Maximum body protein (189.8 g kg^?1) was also obtained in fish fed above diet. Highest haematocrit value (35%), Hb concentration (9.54 g dL^?1), RBC count (3.44 × 10⁹ mL^?1) and lowest Erythrocyte sedimentation rate (ESR) (1.93 mm h^?1) were obtained at the above level of arginine in the diet. AWG, FCR, PRE% and ERE% data were analysed using broken‐line and an exponential fit to obtain more precise dietary arginine requirement. On the basis of broken‐line and exponential analyses of AWG, FCR, PRE and ERE data, inclusion of dietary arginine in the range of 20.4–22.6 g kg^?1 dry diet, corresponding to 51–56.5 g kg^?1 dietary protein, is recommended for formulating arginine‐balanced feeds for rearing H. fossilis fry.     

Quantitative dietary leucine requirement of juvenile Pacific white shrimp,Litopenaeus vannamei (Boone) reared in low‐salinity water

The experiment was conducted to determine the leucine requirement of juvenile Pacific white shrimp Litopenaeus vannamei (Boone) in low‐salinity water (0.50–1.20 g L^?1). Six diets were formulated to contain 410 g kg^?1 crude protein with fish meal, peanut meal and precoated crystalline amino acids with different concentration of l ‐leucine (16.72, 19.60, 22.06, 24.79, 27.28 and 30.16 g kg^?1 dry diet). Each diet was randomly assigned to triplicate groups of 30 shrimps (0.38 ± 0.002 g), and the feed trial lasted for 8 weeks. The results indicated that the maximum weight gain was observed at 24.95 g kg^?1 dietary leucine group, whereas the diets containing higher leucine concentration conversely reduced the growth performance (P < 0.05). Moreover, the highest body protein content and body protein deposition and the lowest haemolymph AST and ALT activities were also found at 24.95 g kg^?1 dietary leucine group. With the increase in leucine in diets, a dose‐dependent increase was found in body lipid content and haemolymph urea concentration. The polynomial regression calculated using weight gain, feed efficiency and body protein deposition indicated that the optimal dietary leucine requirement for L. vannamei reared in low‐salinity water was 23.73 g kg^?1 leucine of dry diet, correspondingly 57.88 g kg^?1 of dietary protein.     

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (Hamilton)

Dietary arginine requirement of fingerling Indian major carp, Cirrhinus mrigala (4.20 ± 0.05 cm; 0.60 ± 0.02 g) was determined by conducting a 8‐week feeding trial with casein–gelatine‐based diets (400 g kg^?1 crude protein; 17.90 kJ g^?1, gross energy), containing crystalline amino acids with graded levels of l ‐arginine (10, 12.5, 15, 17.5, 20 and 22.5 g kg^?1, dry diet). Fish were randomly stocked, in triplicate groups, in 55‐L indoor polyvinyl flow through circular tanks and fed experimental diets at 5% of their body weight divided into two feedings at 08.00 and 16.00 hours. Live weight gain (321%) and feed conversion ratio (FCR 1.40) were significantly (P < 0.05) higher in fish fed diet containing 17.5 g kg^?1dietary arginine compared with other diets. Second‐degree polynomial regression analysis of live weight gain, FCR and protein efficiency ratio data indicated requirements for dietary arginine at 18.7, 18.4 and 18.3 g kg^?1 of the dry diet, respectively. Maximum carcass protein, and minimum moisture and fat contents were noticed at the requirement level. Carcass ash content remained insignificantly different among the treatments except at 17.5 g kg^?1 dietary arginine showing significantly higher ash content. Based on the above results, it is recommended that the diet for fingerling C. mrigala should contain arginine at 18.4 g kg^?1, dry diet, corresponding to 46 g kg^?1 dietary protein for optimum growth and efficient feed utilization.     

Dietary threonine requirement of fingerling Indian major carp,Labeo rohita (Hamilton)

An 8‐week feeding experiment was conducted in a water flow‐through system (26–28 °C) to determine the dietary threonine requirement of fingerling Labeo rohita (3.90±0.03 cm; 0.58±0.02 g). Growth, feed utilization and body composition of fish fed test diets (40% crude protein; 17.9 kJ g^?1 gross energy) with graded levels of l ‐threonine (0.75%, 1.0%, 1.25%, 1.50%, 1.75% and 2.0% dry diet) to apparent satiation were response variables used to assess threonine adequacy. Diets were made isonitrogenous and isoenergetic by adjusting the levels of glycine and dextrin. The amino acid profiles of the test diets were formulated to that of 40% whole chicken egg protein except for threonine. The performance of fish fed experimental diets was evaluated using calculated values for weight gain (g fish^?1), feed conversion ratio (FCR), protein efficiency ratio (PER) and protein productive value (PPV) data. Maximum weight gain (g fish^?1) (1.79), lowest FCR (1.39), highest PER (1.76) and PPV (0.33) were recorded at 1.50 g per 100 g dietary threonine. Statistical analysis of weight gain, FCR, PER and PPV data reflected significant differences (P<0.05) among treatments. Except for reduced growth performance in fish fed threonine‐deficient diets, no deficiency signs were noted. Weight gain, FCR, PER and PPV data were also analysed using second‐degree polynomial regression analysis to obtain a more accurate threonine requirement estimate, which was found, using each response variable, to be at 1.70, 1.63, 1.65 and 1.51 g per 100 g of dry diet, corresponding to 4.2, 4.07, 4.12 and 3.77 g per 100 g of dietary protein respectively. Based on the second‐degree polynomial regression analysis of the live weight gain, FCR, PER and PPV data, the optimum dietary level of threonine for fingerling L. rohita was found to be in the range of 1.51–1.70 g per 100 g of the dry diet, corresponding to 3.77–4.2 g per 100 g of dietary protein.     

Dietary thiamin and pyridoxine requirements of fingerling Indian major carp,Cirrhinus mrigala (Hamilton)

Two experiments were conducted to quantify the dietary thiamin (experiment I) and pyridoxine (experiment II) requirements of fingerling Cirrhinus mrigala for 16 weeks. In experiment I, dietary thiamin requirement was determined by feeding seven casein–gelatin‐based diets (400 g kg^?1 CP; 18.69 kJ g^?1 GE) with graded levels of thiamin (0, 0.5, 1, 2, 4, 8 and 16 mg kg^?1 diet) to triplicate groups of fish (6.15 ± 0.37 cm; 1.89 ± 0.12 g). Fish fed diet with 2 mg kg^?1 thiamin had highest specific growth rate (SGR), protein retention (PR), RNA/DNA ratio, haemoglobin (Hb), haematocrit (Hct), RBCs and best feed conversion ratio (FCR). However, highest liver thiamin concentration was recorded in fish fed 4 mg thiamin kg^?1 diet. Broken‐line analysis of SGR, PR and liver thiamin concentrations exhibited the thiamin requirement in the range of 1.79–3.34 mg kg^?1 diet (0.096–0.179 μg thiamin kJ^?1 gross energy). In experiment II, six casein–gelatin‐based diets (400 g kg^?1 CP; 18.69 kJ g^?1 GE) containing graded levels of pyridoxine (0, 2, 4, 6, 8 and 10 mg kg^?1 diet) were fed to triplicate groups of fish (6.35 ± 0.37 cm; 1.97 ± 0.12 g). Fish fed diet containing 6 mg kg^?1 pyridoxine showed best SGR, FCR, PR, RNA/DNA ratio, Hb, Hct and RBCs, whereas maximum liver pyridoxine concentration was recorded in fish fed 8 mg kg^?1 dietary pyridoxine. Broken‐line analysis of SGR, PR and liver pyridoxine concentrations reflected the pyridoxine requirement from 5.63 to 8.61 mg kg^?1 diet. Data generated during this study would be useful in formulating thiamin‐ and pyridoxine‐balanced feeds for the intensive culture of this fish.     

Dietary amino acid l‐methionine requirement of fingerling Indian catfish,Heteropneustes fossilis (Bloch‐1974) estimated by growth and haemato‐biochemical parameters

An 8 weeks feeding trial was conducted to determine the dietary methionine requirement of fingerling Indian catfish, Heteropneustes fossilis (6.08 ± 0.95 cm; 4.33 ± 0.52 g). Six isonitrogenous (40%) and isoenergetic (17.90 kJ g^?1 GE) amino acid test diets were formulated with gradation of 0.25 g 100 g^?1containing graded levels of _L‐methionine (0.30, 0.55, 0.80, 1.05, 1.30 and 1.55 g 100 g^?1, dry diet) with 0.40 g 100 g^?1 constant level of cystine. Twenty fish were stocked in triplicate groups, in 75‐L circular trough with continuous flow‐through system and fed experimental diets at 4% BW/day twice daily, at 08:00 and 18:00 hours. Maximum live weight gain (296%), best feed conversion ratio (1.56) and protein efficiency ratio (1.60) were occurred at 1.05 g 100 g^?1 methionine, beyond which they showed declining tendency. However, quadratic regression analysis of weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER) and body protein deposition (BPD) data indicated requirement for methionine at 1.15, 1.08, 1.06 and 1.05 g 100 g^?1 of dry diet respectively. Significantly (P < 0.05), higher whole body protein content, minimum moisture and intermediate fat contents were recorded at 1.05 g 100 g^?1 dietary methionine level. Ash content remained insignificantly (P > 0.05) low among all the treatments, excepting at diet I and diet II. Body protein deposition was also found to be significantly (P < 0.05) higher at 1.05 g 100 g^?1 methionine level. Best somatic and haematological indices values were also obtained at the requirement level. Based on above results, it is recommended that the diet for young H. fossilis should contain methionine at 1.09 g 100 g^?1 dry diet, corresponding to 2.73 g 100 g^?1 dietary protein with 0.40 g 100 g¹ cystine concentration for optimum growth and efficient feed utilization. Thus, the total sulphur amino acid requirement of H. fossilis would be (1.09 + 0.40) 1.49 g 100 g^?1 of dry diet, corresponding to 3.73 g 100 g^?1 of dietary protein.     

Dietary isoleucine requirement of fingerling Indian major carp, Labeo rohita (Hamilton)

An 8‐week feeding experiment was conducted to quantify the dietary isoleucine requirement of fingerling Indian major carp, Labeo rohita (3.50 ± 0.04 cm; 0.40 ± 0.02 g) using amino acid test diets (400 g kg⁻¹ crude protein; 17.90 kJ g⁻¹ gross energy) containing casein, gelatin and l ‐crystalline amino acids. Six dietary treatments supplemented with graded levels of isoleucine (7.5, 10.0, 12.5, 15.0, 17.5 and 20.0 g kg⁻¹), in gradations of 2.5 g kg⁻¹ diet, were fed to triplicate groups of fingerlings to apparent satiation divided over two feedings at 07:00 and 17:30 h. Performance of the fish was evaluated on the basis of live weight gain, feed conversion ratio (FCR), protein efficiency ratio (PER), specific growth rate (SGR) and protein productive value (PPV). Statistical analysis of live weight gain, FCR, PER, SGR and PPV reflected significant differences among treatments. Live weight gain and conversion efficiencies were best with isoleucine at 15.0 g kg⁻¹ of diet. Live weight gain, FCR, PER, SGR and PPV data were also analysed using second‐degree polynomial regression analysis to obtain more accurate isoleucine requirement estimate which was found to be at 15.9, 15.3, 15.2, 15.8 and 15.7 g kg⁻¹ of dry diet, corresponding to 39.8, 38.3, 38.0, 39.5 and 39.3 g kg⁻¹ of dietary protein respectively. Based on the quadratic regression analysis of the live weight gain, FCR, PER, SGR and PPV, the optimum level of isoleucine for fingerling L. rohita is in the range of 15.2–15.9 g kg⁻¹ of dry diet, corresponding to 38.0–39.8 g kg⁻¹ of dietary protein. Maximum body protein, minimum moisture and fat were noted at 15.0 g kg⁻¹ of dietary isoleucine while the body ash remained constant among all the treatment levels. No mortality was recorded during the duration of the experiment.     

Growth performance,oxidative stress indices and hepatic carbohydrate metabolic enzymes activities of juvenile Nile tilapia,Oreochromis niloticus L., in response to dietary starch to protein ratios

The effect of various dietary starch to proteins ratios (STA/P) on growth performance, oxidative status and liver enzyme activities involved in intermediary metabolism in juvenile Nile tilapia was evaluated. Four isocaloric‐practical diets (12.73 MJ kg^?1 digestible energy) with increasing STA/CP ratios were formulated. These were designated D₀ (344 g crude protein (CP) and 163.5 g starch (STA) kg^?1), D₁ (310 g CP and 243 g STA kg^?1), D₂ (258 g CP and 322 g STA kg^?1) and D₃ (214 g CP and 401 g STA kg^?1). Each diet was fed to triplicate groups of 60 fish (2.7 g) for 45 days. Compared with the control diet (D₀), significantly (P < 0.05) depressed growth and feed efficiency were observed only in the groups fed on diet D₃. The activities of hepatic enzymes involved in glycolysis and lipogenesis pathways were significantly enhanced in groups fed on diet D₃ compared with other diets. A significant (P < 0.05) increase in catalase activity was detected only in groups fed on diet D₃. Similarly, a significant (P < 0.05) enhancement in superoxyde dismutase, glutathione S‐transferases and glutathione peroxidise was observed in groups fed on diets D₂ and D₃ compared with other diets. Results demonstrate the ability of juvenile Nile tilapia to spare protein by dietary carbohydrate.     

Protein requirement of silver barb, Puntius gonionotus fingerlings

Five iso‐energetic (15.05 MJ kg^?1) semi‐purified diets with graded levels of crude protein, i.e. 200 (D‐1), 250 (D‐2), 300 (D‐3), 350 (D‐4) and 400 (D‐5) g kg^?1 diet were fed to Puntius gonionotus fingerlings (average weight 0.88 ± 0.03 g) in triplicate groups (15 healthy fish per replicate) for a period of 90 days to determine the optimum protein requirement of the fish. Fifteen flow‐through cement tanks of 100‐L capacity with a flow rate of 0.5 L min^?1 were used for rearing the fish. Specific growth rate (SGR), food conversion (food gain) ratio (FCR), nutrient digestibility and retention, digestive enzyme activity, RNA : DNA ratio and tissue composition were used as response parameters with respect to dietary protein levels and feed intake. The mean weight gains of fish after 90 days were 10.84 ± 0.27, 11.07 ± 0.12, 14.09 ± 0.20, 11.27 ± 0.12 and 10.91 ± 0.25 g for D‐1, D‐2, D‐3, D‐4 and D‐5, respectively. Maximum SGR (3.13 ± 0.02% per day), RNA : DNA ratio (10.09 ± 0.09), tissue protein content (160 ± 0.1 g kg^?1 wet weight), protease activity (25.27 ± 0.47 μg of leucine liberated mg tissue per protein h^?1 at 37 °C) and minimum FCR (1.60 ± 0.02) was found in D‐3 group fed with 300 g kg^?1 protein level. All these parameters were negatively affected with the further increase in protein level in the diet. Digestibility of protein, lipid and energy was not affected because of variation in dietary protein levels and nitrogen intake of fish. Maximum energy retention (27.68 ± 0.12%) was recorded at 300 g kg^?1 dietary crude protein fed group. However, using broken line regression analysis, the maximum growth was found to be at 317.7 g kg^?1 dietary protein. Hence, it may be concluded that the protein requirement of P. gonionotus fingerling is 317.7 g kg^?1 diet with a resultant P/E ratio of 21.1 g protein MJ^?1.     

Effect of dietary l‐lysine levels on growth,feed conversion,lysine retention efficiency and haematological indices of Heteropneustes fossilis (Bloch) fry

Effect of varying dietary lysine levels on growth, feed conversion, nutrient retention, lysine retention efficiency and haematological indices of Heteropneustes fossilis fry (2.97 ± 0.11 cm; 4.78 ± 0.31 g) was studied by conducting a 12‐week feeding trial. Isonitrogenous (450 g kg^?1 CP) and isocaloric (17.97 kJ g^?1 GE) amino acid test diets with graded concentrations of l ‐lysine (18, 20, 22, 24, 26, 28 g kg^?1 dry diet) were fed to triplicate groups of fish to apparent satiation twice daily at 17 and 17:30 h. Maximum thermal growth coefficient (TGC, 0.82), best feed conversion ratio (FCR, 1.28) highest protein retention efficiency (PRE, 36%), energy retention efficiency (ERE, 79%) and lysine retention efficiency (LRE, 75%) were noted at 24 g kg^?1 lysine of dry diet. Body protein was also found to be in line with growth data and peaked at 24 g kg^?1 lysine of dry diet. Similarly, superior somatic and haematological indices were exhibited by the groups fed dietary lysine at 24 g kg^?1 of the dry diet. However, exponential analysis of dietary lysine intake against TGC, lysine retention and protein retention indicated that inclusion of dietary lysine in the range of 13.24–14.14 g kg^?1 dry diet, corresponding to 29.42–31.42 g kg^?1 dietary protein, is essential for faster growth of this fish.     

Dietary tryptophan requirement of fingerling Catla catla (Hamilton) based on growth,protein gain,RNA/DNA ratio,haematological parameters and carcass composition

A 12‐week feeding trial was conducted in eighteen 70 L indoor polyvinyl circular troughs provided with a water flow‐through system (1–1.5 L min^?1) at 28 ± 1 °C to evaluate the dietary tryptophan requirement of fingerling Catla catla (3.45 ± 0.24 cm; 0.60 ± 0.13 g). Six casein‐gelatin‐based amino acid test diets (330 g kg^?1 crude protein; 13.6 kJ g^?1 digestible energy) containing graded levels of L‐tryptophan (1.0, 1.4, 1.9, 2.3, 2.8, 3.4 g kg^?1 dry diet) were fed to triplicate groups of fish near to satiation at 08:00, 12:30 and 17:30 h. Absolute weight gain, feed conversion ratio, protein gain, RNA/DNA ratio, hepatosomatic index, viscerosomatic index, condition factor and haematological indices improved with the increasing levels of tryptophan from 1.0 to 2.3 g kg^?1 of dry diet. Significantly higher carcass protein was obtained at 2.3 g tryptophan per kilogram of the dry diet. Exponential analysis of absolute weight gain, feed conversion ratio, protein gain and RNA/DNA ratio against dietary tryptophan levels at 95% maximum and minimum responses displayed the tryptophan requirement at 2.5, 2.3, 2.5 and 2.1 g kg^?1 dry diet, respectively. Inclusion of dietary tryptophan in the range of 2.1–2.5 g kg^?1 dry diet, equivalent to 6.4–7.6 g kg^?1 dietary protein, is recommended in formulating tryptophan‐balanced feed for the culture of this fish species.     

Dietary vitamin E requirement for maximizing the growth,conversion efficiency,biochemical composition and haematological status of fingerling Channa punctatus

The effect of feeding graded levels of vitamin E (E₀, E₂₀, E₄₀, E₆₀, E₁₀₀, E₁₄₀, E₁₈₀, E₂₂₀, E₂₆₀) in nine casein–gelatin‐based isonitrogenous (450 g kg^?1 crude protein) and isoenergetic (17.97 kJ g^?1 gross energy) experimental diets was evaluated in fingerling Channa punctatus for 12 weeks. Growth, nutritional and haematological parameters were studied. Hepatic lipid peroxidation as thiobarbituric acid‐reactive substances (TBARS) was also assayed. The maximum absolute weight gain (AWG g/fish, 55), best feed conversion ratio (FCR, 1.32), protein retention efficiency (PRE, 40%) and energy retention efficiency (ERE, 76%) were achieved in fish fed on a diet supplemented with 140 mg vitamin E kg^?1 diet (E₁₄₀). A consistent decline in the hepatic TBARS concentration and an improvement in haematocrit (Hct) and haemoglobin (Hb) were displayed in fish fed on diets with increasing concentrations of vitamin E up to 140 mg kg^?1 (E₀–E₁₄₀), beyond which (E₁₈₀–E₂₆₀) a reverse trend in these parameters was evident. Based on the broken‐line regression and exponential analyses of AWG, FCR, PRE, ERE, Hb and Hct data, diets for fingerling C. punctatus should contain vitamin E in the range of 140–169 mg kg^?1 to maintain satisfactory fish performance.