scholarly journals The effect of a dacitic tuff breccia (Azomite®) in corn, soybean, and DDGS based diets that vary in inorganic phosphate source on pellet mill production rate and pellet quality

Author(s):  
T.P. Boltz ◽  
J. Ferrel ◽  
K.M. Bowen ◽  
K.L. Harding ◽  
V.E. Ayres ◽  
...  
Author(s):  
C. E. Evans ◽  
R. J. Beeman ◽  
M. Saensukjaroenphon ◽  
C. B. Paulk ◽  
C. R. Stark

2015 ◽  
Vol 1130 ◽  
pp. 543-546 ◽  
Author(s):  
A.J. Murray ◽  
Sarah Singh ◽  
M.R. Tolley ◽  
L.E. Macaskie

Rare earth elements (REEs) are highly valuable due to the complex nature of their extraction from primary and secondary sources. A key feature is that REEs often co-occur with uranium and thorium which, being radioactive, increase the hazard and complexity of REE recovery. A bioprocess which utilizes enzymatically-generated inorganic phosphate to precipitate REEs from solution as their phosphate biominerals is highly effective in the recovery of REEs, effecting rapid recovery onto immobilized bacterial biofilm at high flow-through rates. This also bioprecipitates U and Th. The metal recovery process requires addition of an organic phosphate substrate, e.g. glycerol 2-phosphate (G2P), the cleavage of which provides the inorganic phosphate source for REE biomineralization. G2P is expensive, precluding its large scale use, but early work using uranium showed that tributyl phosphate (TBP) can be used as an alternative phosphate donor molecule. The potential for substitution of G2P by TBP for biorecovery of neodymium is described and a new approach is proposed for enhancing the metal selectivity for REEs against uranium.


2020 ◽  
Vol 98 (Supplement_3) ◽  
pp. 179-179
Author(s):  
Gage E Nichols ◽  
Charles R Stark ◽  
Aundria Ogles ◽  
Kara M Dunmire ◽  
Chad B Paulk

Abstract The objective of this experiment was to determine the effect of conditioning temperature on pellet durability index (PDI) and pellet hardness. A nursery pig diet was formulated to contain 25% spray-dried whey. Treatments consisted of three different conditioning temperatures: 54, 63, and 71°C. Diets were steam conditioned (245 mm × 1397 mm Wenger twin staff pre-conditioner, Model 150) for approximately 30 sec and pelleted using a 1-ton 30-horsepower pellet mill (1012-2 HD Master Model, California Pellet Mill) with a 4.8 mm × 31.8 mm pellet die (L:D 6.7). The production rate was set at 900 kg/h. Treatments were pelleted at 3 separate time points to provide 3 replicates per treatment. Samples were collected directly after discharging from the pellet mill and cooled in an experimental counterflow cooler. Samples were analyzed for PDI using the Holmen NHP 100 for 60 sec (TekPro Ltd, Norfolk, UK). Pellet hardness was determined by evaluating the peak amount of force applied before the first signs of fracture. Although conditioning temperature was increased in a linear fashion, a quadratic increase (P < 0.002) in hot pellet temperature (HPT) was observed. The HPT were 68, 72, and 74°C for diets conditioned to 54, 63 and 71°C, respectively. Increasing conditioning temperature resulted in increased (linear, P < 0.045) PDI and pellet hardness. As conditioning temperature increased from 54, to 71°C PDI increased from 87% to 92% and the force required to crush pellets increased from 13.5 to 15.9 kg. There was a tendency for a correlation (P < 0.076, r = 0.618, r2 = 0.382) between pellet hardness and PDI. Overall, increasing the conditioning temperature increased pellet hardness and pellet durability.


2020 ◽  
Vol 202 (22) ◽  
Author(s):  
Jessica L. Kelliher ◽  
Aleeza J. Leder Macek ◽  
Kevin M. Grudzinski ◽  
Jana N. Radin ◽  
Thomas E. Kehl-Fie

ABSTRACT Phosphate is an essential nutrient that Staphylococcus aureus and other pathogens must acquire from the host during infection. While inorganic monophosphate (Pi) is the preferred source of this nutrient, bacteria can also obtain it from phosphate-containing organic molecules. The Pi-responsive regulator PhoPR is necessary for S. aureus to cause infection, suggesting that Pi is not freely available during infection and that this nutrient must be obtained from other sources. However, the organophosphates from which S. aureus can obtain phosphate are unknown. We evaluated the ability of 58 phosphorus-containing molecules to serve as phosphate sources for S. aureus. Forty-six of these compounds, including phosphorylated amino acids, sugars, and nucleotides, supported growth. Among the organophosphate sources was glycerol-3-phosphate (G3P), which is commonly found in the mammalian host. Differing from the model organism Escherichia coli, S. aureus does not import G3P intact to obtain Pi. Instead, S. aureus relies on the phosphatase PhoB to release Pi from G3P, which is subsequently imported by Pi transporters. To determine if this strategy is used by S. aureus to extract phosphate from other phosphate sources, we assessed the ability of PhoB- and Pi transporter-deficient strains to grow on the same library of phosphorus-containing molecules. Sixty percent of the substrates (28/46) relied on the PhoB/Pi transporter pathway, and an additional 10/46 (22%) were PhoB independent but still required Pi transport through the Pi transporters. Cumulatively, these results suggest that in Pi-limited environments, S. aureus preferentially generates Pi from organophosphates and then relies on Pi transporters to import this nutrient. IMPORTANCE For bacteria, the preferred form of the essential nutrient phosphate is inorganic monophosphate (Pi), but phosphate can also be extracted from a variety of phosphocompounds. Pathogens, including Staphylococcus aureus, experience Pi limitation within the host, suggesting that the use of alternative phosphate sources is important during infection. However, the alternative phosphate sources that can be used by S. aureus and others remain largely unexplored. We screened a library of phosphorus-containing compounds for the ability to support growth as a phosphate source. S. aureus could use a variety of phosphocompounds, including nucleotides, phosphosugars, and phosphoamino acids. Subsequent genetic analysis determined that a majority of these alternative phosphate sources are first processed extracellularly to liberate Pi, which is then imported through Pi transporters.


1971 ◽  
Vol 18 (2) ◽  
pp. 153-166 ◽  
Author(s):  
Jane North ◽  
D. Lewis

SUMMARY1.Coprinus lagopusproduces two non-specific phosphatases: a constitutive acid phosphatase, and an alkaline phosphatase which is repressed during growth on media with a high inorganic phosphate concentration.2. The alkaline phosphatase is also repressed whenCoprinusis grown on an organic phosphate source; but if the acid phosphatase is selectively inhibited by fluoride the alkaline phosphatase is de-repressed and growth is comparable to that observed on an inorganic phosphate source.3. Alkaline phosphatase is not repressed in aerial mycelium or sporophores even when grown on high phosphate medium.4. Mutants altered in their capacity to synthesize alkaline phosphatase were selected from two compatible wild-type strains, H2 and H5.5. Mutants producing a higher level of alkaline phosphatase than wild-type (‘regulator’ mutants) fall into four (or possibly five) complementation groups. Assuming five separate genes, two pairs are linked; the remaining one is independent and on another chromosome.6. Mutants deficient in alkaline phosphatase synthesis fall into at least three groups. They were tested for linkage to ‘regulator’ loci but so far there is no evidence of this.


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