Summary We have analyzed the products formed when mixtures of a nucleoside and ammonium dihydrogen phosphate are heated with an excess of urea. If there is more phosphate than nucleoside in the mixture, compounds containing pyrophosphate bonds are obtained. If uridine, as nucleoside, is in excess over phosphate, di- and oligonucleotides are formed.On leave from Department of Medical Biochemistry, University of Göteborg, Sweden. 相似文献
Four rumen and duodenum cannulated, Holstein lactating cows were used in a change-over design to determine the effects of NaOH, formaldehyde (HCHO) or urea treated barley on disappearance of dry matter (DM), crude protein (CP), amino acids (AA), NDF, ADF and starch of barley in the rumen, post-abomasal (PAT) and total tract by the mobile nylon bag technique. Experimental treatments were coarse milled barley, barley treated with 35 g NaOH/kg, barley treated with 4 g formaldehyde/kg and barley treated with 35 g urea/kg, in which all chemical treated barley was milled coarse before feeding.
NaOH treatment reduced concentrations of lysine and cystine in the barley grain. All chemical treatments decreased rumen disappearances of barley CP but only NaOH and formaldehyde treatments also decreased total AA and some of the AA disappearances in the rumen. All chemical treatments increased DM, OM, CP, starch, NDF and ADF disappearance of barley in the PAT, but only NaOH and formaldehyde treatments increased total AA and most individual AA disappearances in the PAT. Chemical treatments increased disappearance of starch, methionine and glycine in the total tract (P<0.05).
Rumen disappearance of TAA was lower than for CP but PAT disappearance of TAA was more than for CP and finally total tract disappearance of TAA was more than for CP. Individual AA in barley disappeared at different rates in the rumen and PAT. Consequently, the proportion of digesta CP and AAs of barley, entering the intestine were changed by the chemical treatments. We concluded that, appropriate treatment of barley with NaOH or HCHO were provided substantial protection of CP and individual AA from rumen digestion and increased disappearance of most of barley nutrients in PAT, but, NaOH treatment reduced the AA quality of barley. Consequently, formaldehyde can therefore be considered better than NaOH and urea for treatment of barley grain. 相似文献
The preparation of 3-oxo-4-azasteroid from A-nor-3,5-secosteroid-3-oic acid is described in a solventless condition catalysed by Lewis acid under microwave irradiation. We utilized urea as an environmentally benign source for the generation of ammonia for the aza cyclization reaction. 相似文献
A multistage well‐mixed model for urea removal from industrial wastewater has been proposed. The model incorporates reaction rate of urea hydrolysis and takes into account the effects of backmixing on the reactor performance. The model provides temperature and concentration distribution of different components along the height of reactor. The predicted data of the model were consistent with the plant data indicating the validity of the model. The impact of different parameters on the performance of urea hydrolyzer has been examined. The result of this work showed that an increase in inlet temperature of wastewater and steam flow rate would improve the urea removal efficiency. 相似文献
A solution of partially N-deacetylated chitosan in aqueous lithium hydroxide (LiOH)/urea was prepared successfully through a freeze-thawing process and the dissolution behavior was studied. The results indicated that chitosan can directly dissolve in LiOH/urea aqueous solution. LiOH mainly contributed to the breakage of intramolecular and intermolecular hydrogen bonds in chitosan. Urea, LiOH, and chitosan formed inclusion compound (IC) with urea as the IC host, and the LiOH-chitosan complex as the guest. Aqueous 4.8 wt % LiOH/8.0 wt % urea was verified to be the optimal solvent for chitosan. The results of rheology and viscosity characterizations revealed that chitosan/4.8 wt % LiOH/8.0 wt % urea aqueous solution was pseudoplastic fluid, and was more stable than the solution of chitosan in acetic acid at ambient temperature. 相似文献
Non-specifically bound nucleic acid contaminants are an unwanted feature of recombinant RNA-binding proteins purified from Escherichia coli (E. coli). Removal of these contaminants represents an important step for the proteins’ application in several biological assays and structural studies. The method described in this paper is a one-step protocol which is effective at removing tightly bound nucleic acids from overexpressed tagged HIV-1 Rev in E. coli. We combined affinity chromatography under denaturing conditions with subsequent on-column refolding, to prevent self-association of Rev while removing the nucleic acid contaminants from the end product. We compare this purification method with an established, multi-step protocol involving precipitation with polyethyleneimine (PEI). As our tailored protocol requires only one-step to simultaneously purify tagged proteins and eliminate bound cellular RNA and DNA, it represents a substantial advantage in time, effort, and expense. 相似文献
Fibroblast growth factor (FGF) 1 is known to be released in response to cellular stress conditions through formation of a multi-protein complex with synaptotagmin 1 and S100A13. In this study, we characterized the denaturant-induced unfolding of synaptotagmin 1, C2A domain in a residue-specific manner by NMR spectroscopy. The amide protons of 30 residues distributed throughout the 3D structure of the whole protein could be followed in a series of 1H-15N HSQC spectra recorded from 0 to 8 M urea under equilibrium conditions. The midpoint for the urea-induced unfolding obtained from NMR coincides with those obtained from steady state fluorescence and CD spectroscopy, revealing that the protein unfolds via a two-state mechanism without accumulating stable intermediates. The thermodynamic parameter obtained from the denaturation curve illustrates the cooperative unfolding of the C2A domain. The implications of C2A domain folding in relation to the release of FGF-1 from the multi-protein complex were discussed. 相似文献