scholarly journals Amino acid digestibility in soybean meal sourced from different regions of the United States and fed to pigs1

2017 ◽  
Vol 95 (2) ◽  
pp. 771-778 ◽  
Author(s):  
K. M. Sotak-Peper ◽  
J. C. González-Vega ◽  
H. H. Stein
2019 ◽  
Vol 97 (Supplement_2) ◽  
pp. 248-248
Author(s):  
Alexandra G McCafferty ◽  
Rebecca M Humphrey ◽  
M Shamimul Hasan ◽  
Mark A Crenshaw ◽  
James Brett ◽  
...  

Abstract Feed is the most expensive component in raising agricultural animals such as pigs in the United States Guar meal is the main by-product from the guar gum production from guar (Cyamopsis tetragonoba) seed. Although said to be unpalatable and possibly toxic, the recently improved products possess promise to be alternative protein-providing feedstuffs for animal industries, primarily because they contain great amounts of protein and are inexpensive. This study was conducted to mainly evaluate the amino acid profile of GuarPro F-81, a newly developed guar meal product in India. Three samples were randomly collected from a production company in India and aliquoted to multiple sub-samples (20 to 200 g/sub-sample), after received, for nutrient evaluation in 2 to 7 laboratories. Results showed that GuarPro F-81 contained (as-fed basis, ±SD) 97.1 ± 1.92% dry matter (n = 7), 57.9 ± 1.29% crude protein (n = 7), 7.17 ± 0.38% crude fat (n = 5), 3.24 ± 1.06% crude fiber (n = 4), 4,440 ± 622 kcal/kg gross energy (n = 2), and 5.40 ± 0.43% ash (n = 5). The amino acid contents (as-fed basis, ±SD, n = 3) were 2.30 ± 0.102% lysine, 0.61 ± 0.032% methionine, 0.68 ± 0.029% cysteine, 1.57 ± 0.009% threonine, 0.80 ± 0.048% tryptophan, 7.43 ± 0.149% arginine, 3.10 ± 0.064% leucine, 1.70 ± 0.095% isoleucine, 1.99 ± 0.073% valine, 1.42 ± 0.075% histidine, 2.14 ± 0.030% phenylalanine, 1.53 ± 0.352% tyrosine, 2.79 ± 0.027% glycine, 2.40 ± 0.190% serine, 1.85 ± 0.108% proline, 2.04 ± 0.015% alanine, 11.14 ± 0.268% glutamic acid, and 5.53 ± 0.096% aspartic acid. While the contents of alanine, cysteine, tyrosine, methionine, valine, phenylalanine, leucine, threonine, isoleucine, lysine, and proline were approximately 0.9 to 27% less than that in soybean meal (a dehulled, solvent extracted product), the contents of serine, aspartic acid, histidine, tryptophan, glutamic acid, glycine, and arginine were approximately 1.8 to 115% higher than those in soybean meal, and so was the crude protein content which was approximately 21.3% higher. While the crude fiber content was approximately 17% less, the crude fat and gross energy contents were approximately 372% and 4% higher than that in soybean meal, respectively.


2017 ◽  
Vol 95 (2) ◽  
pp. 771 ◽  
Author(s):  
K. M. Sotak-Peper ◽  
J. C. González-Vega ◽  
H. H. Stein

2005 ◽  
Vol 79 (17) ◽  
pp. 11412-11421 ◽  
Author(s):  
Chang-Won Lee ◽  
David E. Swayne ◽  
Jose A. Linares ◽  
Dennis A. Senne ◽  
David L. Suarez

ABSTRACT In early 2004, an H5N2 avian influenza virus (AIV) that met the molecular criteria for classification as a highly pathogenic AIV was isolated from chickens in the state of Texas in the United States. However, clinical manifestations in the affected flock were consistent with avian influenza caused by a low-pathogenicity AIV and the representative virus (A/chicken/Texas/298313/04 [TX/04]) was not virulent for experimentally inoculated chickens. The hemagglutinin (HA) gene of the TX/04 isolate was similar in sequence to A/chicken/Texas/167280-4/02 (TX/02), a low-pathogenicity AIV isolate recovered from chickens in Texas in 2002. However, the TX/04 isolate had one additional basic amino acid at the HA cleavage site, which could be attributed to a single point mutation. The TX/04 isolate was similar in sequence to TX/02 isolate in several internal genes (NP, M, and NS), but some genes (PA, PB1, and PB2) had sequence of a clearly different origin. The TX/04 isolate also had a stalk deletion in the NA gene, characteristic of a chicken-adapted AIV. By analyzing viruses constructed by in vitro mutagenesis followed by reverse genetics, we found that the pathogenicity of the TX/04 virus could be increased in vitro and in vivo by the insertion of an additional basic amino acid at the HA cleavage site and not by the loss of a glycosylation site near the cleavage site. Our study provides the genetic and biologic characteristics of the TX/04 isolate, which highlight the complexity of the polygenic nature of the virulence of influenza viruses.


1995 ◽  
Vol 15 (5_suppl) ◽  
pp. 67-74 ◽  
Author(s):  
Michael R. Jones

In regard to the question posed in the title of this review, the answer is mixed. IPN is possible today but only on a limited basis and at high cost with uncertain benefit. A 1.1% amino acid dialysis solution for IPAA therapy is available in several European countries but has not yet been approved for use in the United States. When it becomes more widely available, IP AA should become an important tool, along with other types of therapy, for use in the maintenance of good nutritional status in PDpatients.


2000 ◽  
Vol 135 (1) ◽  
pp. 101-101

Clarke, E. J. and Wiseman, J. Developments in plant breeding for improved nutritional quality of soya beans I. Protein and amino acid content. Volume 134, part 2, pp. 111–124.Clarke, E. J. and Wiseman, J. Developments in plant breeding for improved nutritional quality of soya beans II. Anti-nutritional factors. Volume 134, part 2, pp. 125–136.The following was omitted from both papers:ACKNOWLEDGEMENTSThe authors are grateful to the United States Soybean Board/American Soybean Association, Dalgety Feed Ltd., Finn Feed International and Pioneer Hi-Bred International for their support.


2000 ◽  
Vol 38 (11) ◽  
pp. 4282-4284 ◽  
Author(s):  
Hyun-Jin Shin ◽  
M. Kariuki Njenga ◽  
Brian McComb ◽  
David A. Halvorson ◽  
Kakambi V. Nagaraja

Nasal turbinates or swabs were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from sentinel ducks placed next to turkey farms experiencing avian pneumovirus (APV) infections and were analyzed for APV genome and infectious particles. APV RNA was detected in samples examined from geese, sparrows, and starlings. APV RNA and antibodies were also detected in two different groups of sentinel ducks. Infectious APV was recovered from sentinel duck samples. The APV M gene isolated from the wild birds had over 96% predicted amino acid identity with APV/Minnesota 2A, which was isolated earlier from domestic turkeys showing respiratory illness, suggesting that wild birds may be involved in spreading APV infection.


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