Mycological Survey of Chicken Feed and Some Feed Ingredients in Turkey

1988 ◽  
Vol 51 (10) ◽  
pp. 807-810 ◽  
Author(s):  
DILEK HEPERKAN ◽  
ÍHSAN ALPERDEN

Level of mold contamination and mycoflora were determined for 144 mixed feed and feed ingredients, including corn, sunflower cake, soja cake, meat and bone meal, and fish meal. Four samples were found to be free of mold. Among the feed samples examined, the mold count has been found to be low (102 to 103 colonies/g) for fish meal, high (104 to 105 colonies/g) for meat-bone meal and sunflower cake, and extremely high (more than 105 colonies/g) for soja cake, corn and mixed feed. The predominant flora in the feed samples consisted of Penicillium, Aspergillus, Fusarium, Mucor and Eurotium, respectively. The most frequently encountered species was found to be Penicillium aurantiogriseum, followed by Aspergillus flavus.

Author(s):  
A.A. Khachankou ◽  
I.V. Katovich ◽  
A.P. Pazyvaila

A comprehensive study of feed staff of animal origin was carried out to identify the most efficient ways of the use as components of compound feeds. In the samples of feeds (fish meal, fish extrudate, meat and bone meal), parameters of nutritional value and safety were determined. It was found that the most stable content of crude protein and essential critical amino acids was characteristic of fish meal, which is advisable to be used for the purpose of balancing compound feed for young animals in protein and lysine.


10.12737/7731 ◽  
2014 ◽  
Vol 9 (4) ◽  
pp. 83-87
Author(s):  
Рудой ◽  
Dmitriy Rudoy

This article presents the results of a study of the amino acid composition of green protein concentrates. The technique of recalculation of formulations for the replacement of expensive protein components by the protein concentrates from green plants. The authors drafted recommendations for replacement such feed ingredients like soy, meat and bone and fish meal by cheaper green protein concentrates. According to the protein content, the soybean is proposed to replace by green protein concentrates of canola, alfalfa, fodder beet; the meat and bone meal by green protein concentrates of canola and alfalfa, fish meal by green protein concentrates of rape.


Author(s):  
JS Jothi ◽  
N Yeasmin ◽  
IZ Anka ◽  
S Hashem

Heavy metals contamination into food chain is considered as an emerging crisis throughout the world especially in developing countries like Bangladesh. The concentration of heavy metals including Cr and Pb in commercial poultry feed samples (protein meal feed, meat and bone meal and fish meal feed) were detected by using Air/ Acetylene Flame Atomic Absorption Spectrophotometer. The mean concentration of heavy metals were found in protein meal feed in a range where Cr 10.63 to 218.10 mg kg-1 and Pb 7.37 to 52.25 mg kg-1. In meat and bone meal feed samples, Cr was recorded from 9.15 to 40.59 mg kg-1 and Pb 5.0 to 61.42 mg kg-1. Cr was found 17.68 to 78.39 mg kg-1 and Pb 3.54to 16.44 mg kg-1 in fish meal feed samples. However, results showed that all feed samples contained chromium and lead where both metals were present at alarming levels in most of the samples. It is therefore suggested that regular detection of heavy metals especially Cr and Pb should be done to evaluate the health risks and to protect the end user from food that might harmful for their health.Int. J. Agril. Res. Innov. & Tech. 6 (2): 57-60, December, 2016


2012 ◽  
Vol 10 (1) ◽  
pp. 169-174
Author(s):  
I Siddika ◽  
M Das ◽  
K R Sumi

A four week experiment was conducted to evaluate the effect of isoproteinous (35%) feed prepared named diet 1, 2, 3 and 4 respectively by substituting 0%, 50% , 75% and 100% fish meal with meat and bone meal in view of preparing a cost effective tilapia (Oreochromis niloticus) fry feed. The four experimental diets (diet 1 to 4) each were randomly assigned to twelve hapas with three replications. Tilapia fry (0.011g) were randomly stocked in 100 fry/9ft² hapa and fed five times a day up to their apparent satiation. The results of the study showed that the weight gain, specific growth rate (SGR), the apparent net protein utilization value and survival (%) of the fish were significantly  (P<0.05) higher and better feed utilization with lower FCR value was observed in fish fed on the diet 4 where meat and bone meal was used as sole source of protein base. There was no significant difference between the carcass moisture and lipid of fish fed with different experimental diets. The results of the study indicated that diet 1 containing fish meal (45.15% Fish meal, 27.43% Rice bran and 27.43% Wheat flour) can be replaced by meat and bone meal containing diet 4 (54.06% Meat and bone meal, 22.97% Rice bran and 22.97% Wheat flour) with no adverse effects on growth and survival of O. niloticus. Before recommendation several trials will be necessary in different farms to be  sure of the reproducibility of the result obtained in the present experiment. Cost- benefit analysis reveals that the   meat and bone meal containing diet certainly provides cheaper feed.   DOI: http://dx.doi.org/10.3329/jbau.v10i1.12110   J. Bangladesh Agril. Univ. 10(1): 169–174, 2012  


2006 ◽  
Vol 3 (4) ◽  
pp. 337-346 ◽  
Author(s):  
Gabriel J. Rensen ◽  
Wayne L. Smith ◽  
Carmela V. Jaravata ◽  
Bennie Osburn ◽  
James S. Cullor

2006 ◽  
Vol 69 (1) ◽  
pp. 205-210 ◽  
Author(s):  
MICHAEL J. MYERS ◽  
HAILE F. YANCY ◽  
MICHAEL ARANETA ◽  
JENNIFER ARMOUR ◽  
JANICE DERR ◽  
...  

A method trial was initiated to validate the use of a commercial DNA forensic kit to extract DNA from animal feed as part of a PCR-based method. Four different PCR primer pairs (one bovine pair, one porcine pair, one ovine primer pair, and one multispecies pair) were also evaluated. Each laboratory was required to analyze a total of 120 dairy feed samples either not fortified (control, true negative) or fortified with bovine meat and bone meal, porcine meat and bone meal (PMBM), or lamb meal. Feeds were fortified with the animal meals at a concentration of 0.1% (wt/wt). Ten laboratories participated in this trial, and each laboratory was required to evaluate two different primer pairs, i.e., each PCR primer pair was evaluated by five different laboratories. The method was considered to be validated for a given animal source when three or more laboratories achieved at least 97% accuracy (29 correct of 30 samples for 96.7% accuracy, rounded up to 97%) in detecting the fortified samples for that source. Using this criterion, the method was validated for the bovine primer because three laboratories met the criterion, with an average accuracy of 98.9%. The average false-positive rate was 3.0% in these laboratories. A fourth laboratory was 80% accurate in identifying the samples fortified with bovine meat and bone meal. A fifth laboratory was not able to consistently extract the DNA from the feed samples and did not achieve the criterion for accuracy for either the bovine or multispecies PCR primers. For the porcine primers, the method was validated, with four laboratories meeting the criterion for accuracy with an average accuracy of 99.2%. The fifth laboratory had a 93.3% accuracy outcome for the porcine primer. Collectively, these five laboratories had a 1.3% false-positive rate for the porcine primer. No laboratory was able to meet the criterion for accuracy with the ovine primers, most likely because of problems with the synthesis of the primer pair; none of the positive control DNA samples could be detected with the ovine primers. The multispecies primer pair was validated in three laboratories for use with bovine meat and bone meal and lamb meal but not with PMBM. The three laboratories had an average accuracy of 98.9% for bovine meat and bone meal, 97.8% for lamb meal, and 63.3% for PMBM. When examined on an individual laboratory basis, one of these four laboratories could not identify a single feed sample containing PMBM by using the multispecies primer, whereas the other laboratory identified only one PMBM-fortified sample, suggesting that the limit of detection for PMBM with this primer pair is around 0.1% (wt/wt). The results of this study demonstrated that the DNA forensic kit can be used to extract DNA from animal feed, which can then be used for PCR analysis to detect animal-derived protein present in the feed sample.


2005 ◽  
Vol 85 (2) ◽  
pp. 185-193 ◽  
Author(s):  
Darryl C Wilkie ◽  
Andrew G Van Kessel ◽  
Lisa J White ◽  
Bernard Laarveld ◽  
Murray D Drew

An experiment was performed to examine the effect of protein source and dietary amino acid profile on intestinal levels of C. perfringens in broiler chickens. Broiler chickens (age = 14 d; n = 192) were fed diets containing 400 g kg-1 crude protein with fish meal, meat/bone meal, feather meal, corn gluten meal, soy protein concentrate, pea protein concentrate, or potato protein concentrate as the primary protein source along with a control diet containing 230 g kg-1 crude protein. The birds were orally inoculated daily, with 1 mL (~1.0 × 108 CFU mL-1) of an overnight culture of C. perfringens between 14 and 21 d of age, killed at 28 d of age and C. perfringens numbers in ileum and cecum were enumerated. Birds fed fish meal, meat/bone meal, feather meal and potato protein concentrate had significantly higher intestinal C. perfringens counts than the birds fed corn gluten meal, soy or pea protein concentrates or the control diet (P < 0.05). The glycine content of the diets and ileal contents was significantly, positively correlated with C. perfringens numbers in ileum and cecum. Dietary glycine may be an important factor in the intestinal overgrowth of C. perfringens in broiler chickens. Key words: Clostridium perfringens, broiler chicken, amino acid, glycine, necrotic enteritis


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