[ON RADIO-GAS CHROMATOGRAPHY OF WHITE PHOSPHORUS AND PHOSPHORUS COMPOUNDS].
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A major QTL for P uptake had previously been mapped to a 13-cM marker interval on the long arm of chromosome 12. To map that major QTL with higher precision and certainty, a secondary mapping population was developed by backcrossing a near-isogenic line containing the QTL from the donor parent to the recurrent parent of low P uptake. Two different mapping strategies have been followed in this study. A conventional QTL mapping approach was based on individual F(2) RFLP data and the phenotypic evaluation of family means in the F(3). The second strategy employed a substitution-mapping approach. Phenotypic and marker data were obtained for 160 F(3) individuals of six highly informative families that differed in the size of donor chromosomal segments in the region of the putative QTL. QTL mapping showed that close to 80% of the variation between families was due to a single QTL, hereafter referred to as Pup1 (Phosphorus uptake 1). Pup1 was placed in a 3-cM interval flanked by markers S14025 and S13126, which is within 1 cM of the position identified in the original QTL mapping experiment. Other chromosomal regions and epistatic effects were not significant. Substitution mapping revealed that Pup1 co-segregated with marker S13126 and that the flanking markers, S14025 and S13752, were outside the interval containing Pup1. The two mapping strategies therefore yielded almost identical results and, in combining the advantages of both, Pup1 could be mapped with high certainty. The QTL mapping appoach showed that the phenotypic variation between families was due to only one QTL without any additional epistacic interactions, whereas the advantage of substitution mapping was to place clearly defined borders around the QTL.
An improved method for the synthesis of cyclic low oxidation state P cations is presented. The only byproducts of the reaction of phosphorus triiodide with chelating phosphines are readily removed, resulting in an easily accessible P(I) reagent with an anion that can be readily replaced through salt metathesis chemistry. These P(I) salts are surprisingly stable, even in O2 and moisture, and the origin of this unusual stability is elucidated using density functional theory calculations.
Hybrids were formed from Bacillus cereus DNA and ribosomal RNA. They were treated with various combination of S1 nuclease and ribonuclease, and the molar ratios of the RNA and DNA moieties remaining in the treated hybrids were determined using a 32P-33P dual-label technique. It was found that both S1 nuclease and ribonuclease are required to give hybrid with RNA and DNA in a perfect 1:1 molar ratio. It was noted that the dual-label technique which employs orthophosphate as the sole phosphorus source for both labels gives unambiguous molar ratios and obviates the need to calculate specific activities, make quench corrections, or correct for base content.
A total of 640 22-wk-old pullets (Shaver SX 288) housed four birds per cage in 40 experimental units (four cages per unit), were randomly assigned eight experimental diets in a 2 x 2 x 2 factorial arrangement. The treatments consisting of two grain sources (wheat and rye) two levels each of crude enzyme preparation (0 and 0.1% Roxazyme G), and added inorganic phosphorus (0 and 0.105%) were fed for five 4-wk periods. At 42 wk of age, 40 individually caged layers were fed the experimental diets with 0.3% chromic oxide (5 individual birds per treatment) to determine AMEn and available P. Plasma P and Ca were also determined. Egg production, feed intake (FI), egg weight, feed efficiency (FE), and specific gravity of eggs were significantly (P < or = 0.05) affected by the experimental periods. Hens fed wheat-based diets had higher (P < or = 0.05) tibia ash (54.3 vs 52.5%), excreta dry matter (22.0 vs 17.7%), and eggshells with > or = 1.080 specific gravity (93.5 vs 89.9%) than birds fed rye. Enzyme supplementation significantly improved AMEn (P < or = 0.01) and FE by 6.2 and 3%, respectively. Egg production increased numerically from 87.6 to 90.1%. Inorganic P supplementation significantly increased egg production (P < or = 0.01), FI, FE, and AMEn (P < or = 0.05) by 4.4, 2, 3, and 2.8%, respectively, but significantly (P < or = 0.05) decreased the proportion of eggs having a specific gravity > or = 1.080 from 92.8 to 90.6%. The enzyme and inorganic P supplementation had no effect on tibia ash content and total plasma Ca and P. Rye can be used in layer rations yielding satisfactory performance when fed with a fungal crude enzyme preparation high in pentosanase/xylanase activity.
Cytoplasmic phosphomonoesters and inorganic phosphate, as well as vacuolar inorganic phosphate and polyphosphates, gave rise to the major peaks in (31)P nuclear magnetic resonance (NMR) spectra of the marine macroalgae Enteromorpha sp., Ceramium sp., and Ulva lactuca which were collected from the sea. In contrast, NMR-visible polyphosphates were lacking in Pylaiella sp. and intracellular vacuolar phosphate seemed to act as the main phosphorus store in this organism. In laboratory experiments, polyphosphates decreased in growing U. lactuca which was cultivated in continuous light under phosphate-deficient conditions. In contrast, the same organism cultivated in seawater with added phosphate and ammonium, accumulated phosphate mainly in the form of polyphosphates. When nitrate was provided as the only nitrogen source, accumulation of polyphosphates in the algae decreased with increasing external nitrate concentration. From the chemical shift of the cytoplasmic Pi peak, the cytoplasmic pH of superfused preparations of Ulva was estimated at 7.2. The vacuolar pH, determined from the chemical shifts of the vacuolar Pi and the terminal polyphosphate peaks, was between 5.5 and 6.0. The intracellular nitrate and ammonium levels in U. lactuca were determined by (14)N NMR. Both nitrogen sources were taken up and stored intracellularly; however, the uptake of ammonium was much faster than that of nitrate.
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