Amino acid and protein supplementation of chick diets containing single cell protein sources1

1973 ◽  
Vol 14 (6) ◽  
pp. 569-578 ◽  
Author(s):  
A. A. Woodham ◽  
P. S. Deans
1982 ◽  
Vol 61 (2) ◽  
pp. 337-344 ◽  
Author(s):  
N.J. DAGHIR ◽  
J.L. SELL

Animals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1676
Author(s):  
Abbas Zamani ◽  
Maryam Khajavi ◽  
Masoumeh Haghbin Nazarpak ◽  
Enric Gisbert

A 60-day trial was conducted in rainbow trout (Oncorhynchus mykiss) fry (initial weight = 2.5 ± 0.6 g) to evaluate the potential use of a bacterial single-cell protein (SCP) as an alternative protein source. Five experimental diets with different levels of fishmeal replacement (0, 25, 50, 75 and 100%) and no amino acid supplementation were tested. At the end of the trial, we found that fry fed diets, replacing 25 and 50% of fishmeal with bacterial SCP, were 9.1 and 21.8% heavier, respectively, than those fed the control diet (p < 0.05), while Feed Conversion Ratio (FCR) values were also lower in comparison to the reference group. These results were also supported by Protein Efficiency Ratio (PER) and Lipid Efficiency Ratio (LER) values that improved in fish fed diets replacing 50% fishmeal by bacterial SCP. The inclusion of SCP enhanced Feed intake (FI) (p < 0.05), although FI was reduced at higher inclusion levels (>50%), which was associated to feed palatability. High levels of bacterial SCP (>50%) affected the muscular amino acid and fatty acid profiles, imbalances that were associated to their dietary content. The broken-line regression analysis using muscle DHA content and weight gain data showed that the maximum levels of fishmeal replacement by bacterial SCP were 46.9 and 52%, respectively.


1988 ◽  
Vol 60 (3) ◽  
pp. 669-682 ◽  
Author(s):  
A. B. McAllan ◽  
J. E. Cockburn ◽  
A. P. Williams ◽  
R. H. Smith

1. Four steers with simple rumen and abomasal cannulas were given diets consisting of ground and pelleted alkali-treated straw, rolled barley and tapioca supplemented with urea (diet U) or containing single-cell protein (diet SCP), maize-gluten meal (diet MGM) or rapeseed meal (diet RSM) in place of some of the tapioca. The isoenergetic diets were given in a 4 x 4 Latin square design in eight feeds/d at 3-h intervals and provided sufficient metabolizable energy to support a growth rate of approximately 0.5 kg/d. Chromic oxide and polyethylene glycol were given as markers and appropriate samples taken from the rumen and abomasum. Flows (g/d) at the abomasum of organic matter and nitrogenous and carbohydrate constituents were calculated.2. Rumen ammonia levels were similar with all three protein supplements at about 9 mmol/l, which was significantly lower (P < 0.05) than that in animals on diet U (16 mmol/l). Rumen liquid outflow rates (/h) were 0.099, 0.139, 0.125 and 0.160 for diets U, SCP, MGM and RSM respectively; the difference between diet U and diet RSM was significant (P < 0.05). Corresponding values for Cr2O3 outflow rates were 0.027, 0.032, 0.027 and 0.030/h respectively, which did not differ significantly from each other.3. RNA, 35S and diaminopimelic acid (DAP) were used as microbial markers. Efficiencies of microbial-N (MN) synthesis, expressed as g MN/kg apparently digestible organic matter, truly digestible organic matter or carbohydrate fermented, were generally not significantly affected by the diet and averaged 29, 22 and 29 respectively based on mean RNA and 35S markers. Corresponding values derived from DAP of 22, 16 and 21 g MN/kg respectively were all significantly (P < 0.001) lower. Using 35S as microbial marker, MN flows at the abomasum as a proportion of non-ammonia-nitrogen flow were 0.78, 0.64, 0.51 and 0.78 for diets U, SCP, MGM and RSM respectively. Derived true rumen degradability values (g/g intake) of the total dietary N were 0.91, 0.79, 0.69 and 0.90 for diets U, SCP, MGM and RSM respectively. Protein supplement degradabilities for single-cell protein, maize-gluten meal and rapeseed meal were 0.73, 0.51 and 0.98 respectively.4. Mouth-to-abomasum digestibility coefficients of the main neutral-sugar components of dietary poly-saccharides were 0.68, 0.63 and 0.61 for arabinose, xylose and cellulose-glucose on diet U. These values were generally significantly increased with protein supplementation, but to different extents depending on the source. Maximum digestibility values of 0.81, 0.79 and 0.76 were obtained for arabinose, xylose and cellulose-glucose with diet RSM. Starch-glucose digestibility was high (0.90) on all diets and unaffected by supplementation.


2022 ◽  
Vol 15 (1) ◽  
Author(s):  
Yang Gu ◽  
Yingying Hu ◽  
Caoxing Huang ◽  
Chenhuan Lai ◽  
Zhe Ling ◽  
...  

Abstract Background Autohydrolysis is an extensively investigated pretreatment method due to its environmental friendliness. During autohydrolysis, most xylan from hemicellulose can be converted into xylooligosaccharides (XOS), and cellulose in the autohydrolyzed residues can be transformed into glucose after enzymatic hydrolysis. Both of these are value-added biochemicals in the biorefining process. In this work, paper mulberry (PM), which contains abundant protein, was utilized as a raw material to coproduce XOS and single-cell protein (SCP) through autohydrolysis and fermentation technologies. Results The results showed that 8.3 g of XOS and 1.8 g of amino acids could be recovered in the autohydrolysate (based on 100 g raw material) after autohydrolysis (170 °C, 1 h). Moreover, 5.7 g of low-DP XOS along with 1.8 g of amino acids could be further obtained from the autohydrolysate after hydrolysis with endo-β-1-4-xylanase. In addition, 20.1 g of fermentable monosaccharides was recovered after hydrolyzing the autohydrolyzed PM with cellulase, which can be used to produce 4.8 g of SCP after fermentation with Candida utilis. Conclusion As a valuable application of PM, a novel process is proposed to coproduce amino acid-rich XOS and SCP through autohydrolysis. The carbohydrate of PM is effectively converted to high value-added products.


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