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Vol.
22, No. 14 Nutrient Characteristics of Pond-Raised Channel Catfish
Edwin H. Robinson, Menghe H. Li, and Daniel F. Oberle IntroductionThe nutrient content of farm-raised channel catfish muscle tissue has been published in part in various research articles over the years; the latest and most comprehensive publication of this kind was that of Nettleton et al. (1990). Generally, the nutrient profile of catfish shows that it is highly nutritious &emdash; high in protein, low in fat and cholesterol, and a good source of certain vitamins and minerals. Over the past 10 years, several changes have been implemented in the channel catfish diet that may affect nutrient composition of the fish. Such changes include an increase in the digestible energy to protein ratio (DE:P) of the diet, a decrease in the concentration of marine fish meal, and a reduction or elimination of certain nutrients in the vitamin and mineral premixes typically used by the catfish feed industry. Also, feeding rates have continued to increase, and this may affect tissue nutrient content. For these reasons, this study was conducted to update information on nutrient content of farm-raised channel catfish muscle tissue. The study also determined liver nutrient concentrations. These data were intended to be used in conjunction with the data from muscle tissue to provide baseline nutritional information that may be useful in assessing the nutritional status of a healthy catfish. MethodsFifty marketable-sized channel catfish were collected from a local catfish processing plant at three times during the growing season (May and October 1998 and February 1999) to evaluate seasonal variation in body composition. The fish were processed with equipment and procedures similar to those used in the catfish processing industry. Muscle (fillet) and liver tissues were collected for analysis of various nutrients. Proximate composition of muscle was determined using AOAC methods (AOAC 1995). Fatty acids in muscle and liver tissues were determined by gas chromatography. Vitamin concentrations were determined by using either microbiological or enzymatic assays or high-pressure liquid chromatography, depending on the vitamin under study. Minerals were analyzed using atomic absorption. Mean and standard deviation of data derived from samples taken in each season and the overall mean and standard deviation of the three seasons were reported. Because the mean fish weights were different in samples taken in the three seasons, the differences in proximate composition that might be caused by the differences in fish weight were corrected by analysis of variance using fish weight as a covariant (Steel and Torrie 1980). ResultsProximate composition of muscle averaged over the three seasons was fairly typical of food-sized channel catfish. Crude protein averaged 16.3 grams per 100 grams of raw tissue (g/100 g); crude fat, 5.4 g/100 g; moisture, 77.3 g/100 g; and ash, 1.1 g/100 g (Table 1). Crude fat was somewhat lower than the 6.9 g/100 g reported by Nettleton et al. (1990). We typically observe significant variation in the fat content of individual catfish, which may be related to genetic variation, diet composition, or feed intake. When fat data from our study were corrected for fish size, fish sampled in the fall contained a higher level of fat compared with fish sampled in the spring or winter. No other seasonal changes in proximate composition were observed. This same trend was previously reported for channel catfish (Nettleton et al. 1990). Mean energy value for muscle tissue from our study was 118 kilocalories per 100 grams of raw tissue (kcal/100 g) (Table 1), which was lower than the 128 kcal/100 g reported by Nettleton et al. (1990) and the 145 kcal/100 g reported by Clement and Lovell (1994). The lower energy value observed in our study appears to be related to the lower level of fat contained within the muscle. The major fatty acids &emdash; which accounted for about 75% of the total &emdash; in fillets were 16:0, 18:0, 18:1, and 18:2 n-6 (Table 2). Concentrations of saturated fatty acids were 23.8% of total lipids; monoenoic, 43.8%; dienoic, 15.3%; and trienoic, 4.1%. These values are typical of those previously reported for catfish (Nettleton et al. 1990; Tidwell and Robinette 1990; Clement and Lovell 1994). Muscle tissue contained 3.7% n-3 fatty acids and 21.5% n-6 fatty acids. These values are within the range generally found in catfish muscle tissue, but their concentrations are dramatically influenced by diet. For example, feeding a source high in n-3 fatty acids (marine fish oil) results in a significant increase in n-3 fatty acids deposited in the tissue. The major fatty acids found in the liver were the same as those found in muscle (Table 3). There were two primary differences between fatty acids in liver and muscle: (1) dienoic was markedly lower in liver; and (2) both n-3 and n-6 highly unsaturated fatty acids were higher in liver. There were some seasonal differences in both liver and muscle fatty acids. For example, n-3 fatty acids were higher in the winter and spring than in early fall. Catfish are fed sparingly during the winter and spring. Tidwell et al. (1992) and Webster et al. (1994) reported that n-3 fatty acids increase in catfish muscle and liver during starvation. They suggested that n-3 fatty acids were conserved for proper physical and metabolic functions. In addition, when feeding is reduced, catfish may consume natural food organisms that are rich in these fatty acids (Robinson and Li 1996). Vitamin concentrations (Table 4) of muscle tissue were similar to values reported by Nettleton et al. (1990). In our study, there were some seasonal variations in tissue concentrations of pantothenic acid and choline. Concentrations of vitamins in liver tissue were generally higher than in muscle, except for thiamin and choline (Table 5). These values were similar to values of pond-raised channel catfish fed a diet containing supplemental vitamins at recommended levels reported by Robinson et al. (1998). These researchers showed that riboflavin, pyridoxine, and folic acid concentrations in catfish liver tissue did not differ between fish fed a diet either with or without supplemental vitamins. Mineral concentrations in muscle (Table 6) were similar to values reported by Nettleton et al. (1990) and Clement and Lovell (1994). No appreciable seasonal variation was observed in mineral concentrations. Pond-raised channel catfish are a good source of phosphorus, potassium, and selenium. Table
1. Proximate nutrient composition and energy value
of the fillet of pond-raised channel catfish
expressed as unit per 100 grams of raw tissue at
three sampling dates.1 Protein
(g) Fat
(g) Moisture
(g) Ash
(g) Energy
(kcal) 2 117 119 118 Fish
weight (g) 685±146 440-974 536±182 358-1098 827±136 588-1238 683±146 Least
square means using live weight as
covariant Protein
(g) 16.6 16.5 15.8 Fat
(g) 5.1 6.1 5.0 Moisture
(g) 77.3 76.2 78.2 Ash
(g) 1.09 1.04 1.02 1Mean
represents 50 fish; SD = Standard Deviation.
Table
2. Fatty acid composition (mean±SD) of the
fillet of pond-raised channel catfish expressed as
percentage of fat.1 Fatty
acid 14:0 16:0 16:1 18:0 18:1 18:2
n-6 18:3
n-6 18:3
n-3 20:1 20:2
n-6 20:3
n-9 20:3
n-6 20:4
n-6 20:5
n-3 22:5
n-6 22:5
n-3 22:6
n-3 Saturated Monoenes Dienes Trienes n-3 n-6 n-3
HUFA2 n-6
HUFA 1Mean
of each sample time represents five composite
samples with 10 fish per sample; SD = Standard
Deviation.
Table
3. Fatty acid composition (mean±SD) of the
liver of pond-raised channel catfish expressed as
percentage of fat.1 Fatty
acid 14:0 16:0 16:1 18:0 18:1 18:2
n-6 18:3
n-6 18:3
n-3 20:1 20:2
n-6 20:3
n-9 20:3
n-6 20:4
n-6 20:5
n-3 22:4
n-6 22:5
n-6 22:5
n-3 22:6
n-3 Saturated Monoenes Dienes Trienes n-3 n-6 n-3
HUFA2 n-6
HUFA
Total
fat 1Mean
of each sample time represents five composite
samples with 10 fish per sample; SD = Standard
Deviation.
Table
4. Concentrations (mean±SD) of selected
vitamins in the fillet of pond-raised channel
catfish expressed as microgram per gram of wet
tissue.1
Vitamin
Thiamin Riboflavin Pyridoxine Folic
acid Niacin Pantothenic
acid Choline Ascorbic
acid 1Mean
of each sample time represents five composite
samples with 10 fish per sample; SD = Standard
Deviation. Table
5. Concentrations (mean±SD) of selected
vitamins in the liver of pond-raised channel
catfish expressed as microgram per gram of wet
tissue.1
Vitamin
Thiamin Riboflavin Pyridoxine Folic
acid Niacin Pantothenic
acid Choline Ascorbic
acid 1Mean
of each sample time represents five composite
samples with 10 fish per sample; SD = Standard
Deviation. Table
6. Concentrations (mean±SD) of selected
minerals in the fillet of pond-raised channel
catfish express as microgram per gram of wet
tissue.1
Mineral
Potassium Phosphorus Sodium Magnesium Calcium Zinc Iron Selenium Copper Manganese Cobalt 1Mean
of each sample time represents three composite
samples with 16-17 fish per sample; SD = Standard
Deviation.
SummaryIn summary, the data presented in this report are intended to provide baseline information on nutrient characteristics of catfish muscle and liver. The muscle nutrient profile shows that channel catfish is highly nutritious &emdash; high in protein, low in fat, and a good source of certain vitamins and minerals. The liver nutritional profile may be useful in assessing the nutritional status of the fish. Further, it appears that the changes that have been implemented in commercial catfish diets during the last few years &emdash; such as a slight increase in the DE:P ratio, a decrease in marine fish meal, and a reduction in the concentrations of supplemental vitamins and minerals &emdash; have not appreciably affected the nutrient composition of the fish. ReferencesAssociation of Official Analytical Chemists International (AOAC). 1995. Official methods of analysis, 16th edition. AOAC, Arlington, Va. Clement, S., and R.T. Lovell. 1994. Comparison of processing yield and nutrient composition of cultured Nile tilapia (Oreochromis niloticus) and channel catfish (Ictalurus punctatus). Aquaculture 119:299-310. Nettleton, J.A., W.H. Allen, Jr., L.V. Klatt, W.M.N. Ratnayake, and R.G. Ackman. 1990. Nutrients and chemical residues in one- to two-pond Mississippi farm-raised channel catfish (Ictalurus punctatus). Journal of Food Science 55:954-958. Robinson, E.H., and M.H. Li. 1996. A practical guide to nutrition, feeds, and feeding: revised. Bulletin 1041, Mississippi Agricultural and Forestry Experiment Station. Robinson, E.H., M.H. Li, and D. Oberle. 1998. Catfish vitamin nutrition. Bulletin 1078, Mississippi Agricultural and Forestry Experiment Station. Steel, R.G., and J.H. Torrie. 1980. Principles and Procedures of Statistics, a Biometric Approach, 2nd Edition. New York, N.Y.: McGraw-Hill. Tidwell, J.H., and H.R. Robinette. 1990. Changes in proximate and fatty acid composition of fillets from channel catfish during a two-year growth period. Transactions of the American Fisheries Society 119:31-40. Tidwell, J.H., C.D. Webster, and J.A. Clark. 1992. Effects of feeding, starvation, and refeeding on the fatty acid composition of channel catfish tissues. Comparative Biochemistry and Physiology 103A:365-368. United States Department of Agriculture (USDA). 1987. Composition of foods: Finfish and shellfish products. Agriculture Handbook No. 8-15, USDA, Washington, D.C. Webster, C.D., J.H. Tidwell, L.S. Goodgame, and D.H. Yancey. 1994. Effects of fasting on fatty acid composition of muscle, liver, and abdominal fat in channel catfish Ictalurus punctatus. Journal of the World Aquaculture Society 25:126-134.
Robinson is a fishery biologist and coordinator of the Thad Cochran National Warmwater Aquaculture Center (NWAC) in Stoneville, Li is an assistant fishery biologist at NWAC, and Oberle is a research assistant at the Delta Research and Extension Center in Stoneville. For more information, contact Robinson at (662) 686-3242; e-mail, ed@drec.msstate.edu. This research report was published by the Office of Agricultural Communications, a unit of the Division of Agriculture, Forestry, and Veterinary Medicine at Mississippi State University.
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