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[Synthesis and antiherpes activity of acyclovir phosphoesters].

9-(Hydroxyethyloxymethyl)guanine (acyclovir) phosphite and fluorophosphate were synthesized by the reactions of acyclovir with phosphorus trichloride in triethyl phosphate and with fluorophosphoric acid in the presence of 2,4,6-triisopropylbenzenesulfonyl chloride, respectively, and characterized by the data of 1H and 31P NMR and mass spectra. These products selectively inhibit reproduction of the herpes simplex virus type 1 in the Vero cell culture, the phosphite being also substantially active against a herpes virus strain resistant to acyclovir.

Acyclovir↗

Phosphorothioate substrates for the SfiI restriction endonuclease.

Oligodeoxynucleotides carrying the recognition sequence for the SfiI endonuclease were synthesised with phosphorothioates at the cleavage site. The Rp and Sp diastereoisomers of the oligonucleotides were separated by HPLC using a mobile phase containing L-cysteine. The duplex with Rp phosphorothioates was cleaved very slowly in the presence of Mg2+, though virtually complete cleavage was obtained with Mn2+. No significant cleavage of the duplex with Sp phosphorothioates occurred with either Mg2+ or Mn2+. When added to a plasmid with one SfiI site, the duplexes with either Rp or Sp phosphorothioates inhibited the rate at which SfiI cleaved the plasmid: a control duplex with oxyester linkages enhanced the rate of plasmid cleavage. In contrast to type IIe nucleases such as EcoRII and NaeI, which can be activated by non-hydrolysable analogues of their substrates, SfiI reactions require four susceptible phosphodiester bonds.

Deoxyribonucleases, Type II Site-Specific↗

Effect of sodium orthovanadate on glycosylation of the phosphopeptidomannans involved in the cell-cell aggregation of the yeast Kluyveromyces bulgaricus.

In studies of yeast flocculation it has been found that low concentrations of vanadium contained in sodium orthovanadate do not affect the growth and the cell-cell adhesion of the yeast Kluyveromyces bulgaricus, whereas high concentrations delay the growth of the yeasts and strongly inhibit flocculation. Moreover, higher sensitivity to Hygromycin B and calcofluor white was taken to imply altered cell wall integrity which is supported by compositional analysis of the extracted phosphopeptidomannans. Yeasts grown on sodium orthovanadate show a decrease in the percentage of phosphopeptidomannans and their compositions. It is proposed that the vanadium contained in sodium orthovanadate has a similar conformation to phosphorus and competes with phosphorus in phosphorylated compounds. The decrease of carbohydrate components and phosphorus linking to phosphopeptidomannans detected may alter their structure and modify ligand binding properties.

Cell Aggregation↗

Phosphorus in prebiotic chemistry.

The prebiotic synthesis of phosphorus-containing compounds-such as nucleotides and polynucleotides-would require both a geologically plausible source of the element and pathways for its incorporation into chemical systems on the primitive Earth. The mineral apatite, which is the only significant source of phosphate on Earth, has long been thought to be problematical in this respect due to its low solubility and reactivity. However, in the last decade or so, at least two pathways have been demonstrated which would circumvent these perceived problems. In addition, recent results would seem to suggest an additional, extraterrestrial source of reactive phosphorus. It appears that the 'phosphorus problem' is no longer the stumbling block which it was once thought to be.

Evolution, Chemical↗

Fractionation of phosphorus and trace elements species in soybean flour and common white bean seeds by size exclusion chromatography-inductively coupled plasma mass spectrometry.

Soluble species of phosphorus, sulfur, selenium and eight metals (Mn, Fe, Co, Ni, Cu, Zn, Mo and Cd) in soybean flour and common white bean seeds were investigated by size exclusion chromatography (SEC) and inductively coupled plasma mass spectrometry (ICP-MS). Samples were extracted by 0.02 mol l(-1) Tris-HCI buffer solution (pH 7.5). Fractionation of sample extracts by preparative scale SEC was accomplished using a Fractogel EMD BioSEC column (600 x 16 mm) and 0.02 mol l(-1) Tris-HCl buffer solution (pH 7.5) as mobile phase (flow rate: 2 ml min(-1)). A 2-ml sample was injected. Contents of elements in chromatographic fractions were determined by AAS, ICP-AES and ICP-MS. The elution profiles of P, Fe, Co, Ni, Cu, Zn and Mo in both samples were similar. Main species of Co, Ni, Cu, Zn and Mo were found in the low molecular weight region (2-5 kDa), whereas Fe is predominantly bound to high molecular weight compounds (180 kDa). The dominant phosphorus fraction was detected in the medium molecular weight region (10-30 kDa) and the other fraction in the low molecular weight region. Isotachophoretic analysis of chromatographic fractions revealed that the main phosphorus compound in the medium molecular weight region is phytic acid. SEC on Superdex 75 and Superdex Peptide columns (300 x 10 mm) was performed in on-line hyphenation with ICP-MS. The same mobile phase was used with a flow rate of 0.5 ml min(-1); volume of injected sample was 200 microl. Element specific chromatograms were obtained by continuous nebulization of effluent into ICP-mass spectrometer measuring intensities of 47(PO)+ and 48(SO)+ oxide ions and 55Mn, 57Fe, 59Co, 62Ni, 65Cu, 66Zn, 82Se, 95Mo and 114Cd nuclides. Chromatographic profiles of elements are generally analogous to those obtained with a Fractogel column, but better chromatographic resolution of separated species was achieved so that slight differences between samples were revealed. Estimated molecular weights of major phosphorus species in soybean flour and common white bean seed extracts are 6 and 3.6 kDa, respectively, whereas those of minor phosphorus species in both samples are 0.7 kDa. Traces of phosphorus were also detected in the high molecular weight region (130 kDa). Chromatograms of P, Ni, Cu, Zn and Mo compounds in both extracts are similar but not identical. Molecular weights of major Cu and Zn species are approximately 1 and 0.4 kDa for soybean flour and white bean seeds, respectively. In cases of Mn, Fe, Co and Se, the element profiles of soybean flour and white bean seed extracts are significantly different.

Chromatography, Gel↗

Sudden infant death syndrome: a possible primary cause.

The hypothesis that poisoning by phosphines, arsines and stibines might be the primary cause of sudden infant death syndrome (SIDS) was investigated. Most mattress materials contain phosphorus or antimony compounds as fire retardant additives. Mattress materials in areas affected by the warmth and perspiration of the sleeping infant were found to be naturally infected by the fungus Scopulariopsis brevicaulis which is thought to be capable of generating phosphines, arsines and stibines from materials containing phosphorus, arsenic or antimony compounds. These gases may cause anticholinesterase poisoning and cardiac failure in infants, but contributory factors include the prone sleeping position and overwrapping. In England and Wales, the progressive increase in SIDS between 1951 and 1988 seems to be related to increasing use of phosphorus and antimony compounds as fire retardents in cot mattresses.

Air Pollutants↗

Chemical characterization and bioavailability of phosphorus in water-insoluble fractions of three mono-ammonium phosphate fertilizers.

Elemental impurities in mono-ammonium phosphate (MAP) fertilizers, such as Fe, Al, Ca, Mg, and F, result in compounds other than NH4H2PO4. The phosphorus availability of the impurity compounds was determined in 3 commercial MAP fertilizers produced from North Carolina, Florida, and Idaho phosphate rocks. Soluble compounds, including NH4H2PO4, were washed out of the fertilizers, and the water-insoluble fraction was collected. The North Carolina, Florida, and Idaho MAP fertilizers contained 13, 16, and 17% water-insoluble fractions, respectively. Availability of phosphorus in each MAP fertilizer and water-insoluble fraction was determined in a greenhouse pot study using sorghum-sudangrass (Sorghum bicolor) as the test crop. There were no differences in dry matter weights or phosphorus uptake between reagent grade MAP and each MAP fertilizer. Lower dry matter weights and phosphorus uptake were produced from the water-insoluble North Carolina, Florida, and Idaho fractions (NC greater than FL greater than ID). Chemical analysis and characterization with optical microscopy, infrared spectroscopy, and X-ray diffractometry indicated 77.3, 73.8, and 73.6% NH4H2PO4 in the North Carolina, Florida, and Idaho MAP fertilizers, respectively. MgAl(NH4)2H(PO4)2F2, AlNH4HPO4F2, and FeNH4(HPO4)2 were identified as water-insoluble phosphorus compounds. There was a significant negative correlation between the percent phosphorus present as MgAl(NH4)2H(PO4)2F2 and the phosphorus availability. Increased crystallinity of the various water-insoluble compounds also contributed to reduced phosphorus availability.

Biological Availability↗

Capture of phosphorus(I) and arsenic(I) moieties by a 1,2-bis(arylimino)acenaphthene (aryl-BIAN) ligand. A case of intramolecular charge transfer.

The reaction of PCl3 with SnCl2 in THF solution, followed by treatment with dpp-BIAN (dpp = 2,6-i-Pr2C6H3), affords the phosphenium complex [(dpp-BIAN)P][SnCl5.THF]. The 31P chemical shift (delta 232.5) and the metrical parameters from a single-crystal X-ray diffraction study indicate that the oxidation state of phosphorus in this compound is +3. A similar conclusion was reached regarding the phosphorus oxidation state in [(dpp-BIAN)P][I3], which was prepared via the reaction of dpp-BIAN with PI3 in CH2Cl2 solution. The arsenium salt [(dpp-BIAN)As][SnCl5.THF] was prepared by treatment of AsCl3 with SnCl2 in THF solution, followed by the addition of dpp-BIAN. The X-ray crystal structure of this salt was determined, and the pattern of bond distances and angles indicates that arsenic is present in the +3 oxidation state.

Journal Article↗

Human primary brain tumour metabolism in vivo: a phosphorus magnetic resonance spectroscopy study.

Magnetic resonance spectroscopy was used to study intracellular pH and compounds which contain phosphorus in normal human brain and primary brain tumours non-invasively. In normal subjects (n = 7) intracellular pH (pHi) of the brain was 7.03 +/- 0.02 (mean +/- s.e.m.). The pHi did not vary between superficial (2 cm, majority grey matter) and deep brain (5 cm, majority white matter). The relative concentrations of phosphocreatine (PCr) and phosphomonoesters (PME) to ATP were also constant with depth. The relative concentration of phosphodiesters (PDE) increased from superficial to deep in normal brain. The astrocytomas (n = 7, grade II-IV) were significantly more alkaline (pHi = 7.08 +/- 0.03), and contained more PCr and PME, with respect to ATP, than normal brain at similar depth. The meningiomas (n = 4) were also more alkaline (pHi = 7.19 +/- 0.02) with a raised PME level but reduced PCr. The reduction in meningioma PCr may be due to the significant necrosis (greater than 20%) seen in the surgical biopsies. No significant necrosis was seen in the gliomas. Previous in vitro studies suggest that increased PME may be due to accumulation of phosphoethanolamine (PE), a phospholipid precursor. These results suggest that human primary brain tumours characteristically are more alkaline with increased PME than normal brain.

Adult↗

[Synthesis of new pyrimidine 5'-H-thiophosphonates].

Thymidine and 3'-deoxythymidine 5'-H-thiophosphonates were synthesized by interaction of 3'-O-acetylthymidine or 3'-deoxythymidine and ammonium phosphinate in the presence of pivaloyl chloride and following oxidation in situ by sulfur of the intermediate phosphinates. The compounds seemed to be 1:1 mixture of diastereomers with chiral phosphorus. The prepared compounds were tested as potential inhibitors of HIV production.

Antiviral Agents↗

[Influence of long-term fertilization on phosphorus fertility of calcareous soil II. Inorganic and organic phosphorus].

By the Jiang-Gu inorganic phosphorus fractionation method and the Bowman-Cole organic phosphorus fractionation method, this paper studied the forms and compositions of inorganic and organic phosphorus in 0-100 cm layer of calcareous soil after 23 years located experiment. The result showed that the content of inorganic phosphorus was in the order of treatment animal manure > fallow > chemical fertilizer > low rate straw > high rate straw > medium rate straw > no fertilizer. The IPi value of inorganic phosphorus forms in different fertilizer treatments had the following characteristics: a) it was relatively low for Ca2-P, Ca8-P and Al-P, but relatively high for Ca10-P, Fe-P and O-P; b) comparing with no fertilizer treatment, treatments animal manure and fallow had a notably high IPi value of Ca2-P, Ca8-P and Al-P and a low IPi value of Ca10-P, Fe-P and O-P; while treatment chemical fertilizer had a high IPi value of Ca2-P, Ca8-P, Al-P and O-P, but a low IPi value of Ca10-P and Fe-P; c) as for available phosphorus source (Ca2-P, Ca8-P and Al-P), their content was higher in treatment animal manure than in treatment chemical fertilizer, and higher in treatment chemical fertilizer than in treatments straws. A combined application of straw and chemical fertilizer could increase soil organic phosphorus content notably. Applying animal manure could increase the content of all organic phosphorus forms, while applying chemical fertilizer could promote the transformation of soil resistant organic phosphorus to labile and medium labile organic phosphorus. No fertilizer treatment had a relatively lower content of labile and medium labile organic phosphorus, but a relatively high content of resistant organic phosphorus. For treatment fallow, it had a relatively low content of soil organic matter and organic phosphorus, but a relatively high content of labile and medium resistant organic phosphorus.

Biomass↗

Phosphorus chemical shift tensors of phosphido ligands in ruthenium carbonyl compounds: (31)P NMR spectroscopy of single-crystal and powder samples and ab initio calculations.

The phosphorus chemical shift (CS) tensors of several ruthenium carbonyl compounds containing a phosphido ligand, micro), bridging a Ru [bond] Ru bond were characterized by solid-state (31)P NMR spectroscopy. As well, an analogous osmium compound was examined. The structures of most of the clusters investigated have approximate local C(2v) symmetry about the phosphorus atom. Compared to the "isolated" PH(2)(-) anion, the phosphorus nucleus of a bridging phosphido ligand exhibits considerable deshielding. The phosphorus CS tensors of most of the compounds have spans ranging from 230 to 350 ppm and skews of approximately zero. Single-crystal NMR was used to investigate the orientation of the phosphorus CS tensors for two of the compounds, Ru(2)(CO)(6)(mu(2)-C [triple bond] C [bond] Ph)(mu(2)-PPh(2)) and Ru(3)(CO)(9)(mu(2)-H)(mu(2)-PPh(2)). The intermediate component of the phosphorus CS tensor, delta(22), lies along the local C(2) axis in both compounds. The least shielded component, delta(11), lies perpendicular to the Ru [bond] P [bond] Ru plane while the most shielded component, delta(33), lies perpendicular to the C [bond]P [bond] C plane. The orientation of the phosphorus CS tensor for a third compound, Ru(2)(CO)(6)(mu(2)-PPh(2))(2), was investigated by the dipolar-chemical shift NMR technique and was found to be analogous, suggesting it to be the same in all compounds. Ab initio calculations of phosphorus magnetic shielding tensors have been carried out and reproduce the orientations found experimentally. The orientation of the CS tensor has been rationalized using simple frontier MO theory. Splittings due to (99,101)Ru [bond] (31)P spin-spin coupling have been observed for several of the complexes. A rare example of (189)Os [bond] (31)P spin-spin splittings is observed in the (31)P MAS NMR spectrum of the osmium cluster, where (1)J((189)Os, (31)P) is 367 Hz. For this complex, the (189)Os nuclear quadrupolar coupling constant is on the order of several hundred megahertz.

Journal Article↗

Sustainable sludge management--what are the challenges for the future?

Sewage sludge is a serious problem due to the high treatment costs and the risks to environment and human health. Future sludge treatment will be progressively focused on an improved efficiency and environmental sustainability of the process. In this context a survey is given of the most relevant sludge treatment options and separate treatment steps. Special attention is paid to those processes that are simultaneously focused on the elimination of the risks for environment and human health and on the recovery or beneficial use of the valuable compounds in the sludge such as organic carbon compounds, inorganic non-toxic substances, phosphorus and nitrogen containing compounds. Also, a brief assessment is given of the specific future technological developments regarding the various treatment steps. Furthermore, it is discussed how to assess the various pathways which can lead to the required developments. In such an assessment the technical and economic feasibility, the environmental sustainability, the societal acceptance and the implementation route are important factors. The optimal approach also strongly depends on the local and regional situation of concern and the relevant current and future boundary conditions.

Carbon↗

Hexaphosphapentaprismane: a new gateway to organophosphorus cage compound chemistry.

Several independent synthetic routes are described leading to the formation of a novel unsaturated tetracyclic phosphorus carbon cage compound tBu4C4P6 (1), which undergoes a light-induced valence isomerization to produce the first hexaphosphapentaprismane cage tBu4C4P6 (2). A second unsaturated isomer tBu4C4P6 (9) of 1 and the bis-[W(CO)5] complex 13 of 1 are stable towards similar isomerization reactions. Another starting material for the synthesis of the hexaphosphapentaprismane cage tBu4C4P6 (2) is the trimeric mercury complex [(tBu4C4P6)Hg]3 (11), which undergoes elimination of mercury to afford the title compound 2. Single-crystal X-ray structural determinations have been carried out on compounds 1, 2, 9, 11, and 13.

Journal Article↗