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1.
Summary The N-metabolism ofArthrocnemum fruticosum (L.) Moq., growing in a saline area north-east of the Dead Sea in Jordan, was studied over its vegetative growth period from
March to September 1981. Plant and soil samples were taken at monthly intervals. Water content, Na+, K+, Cl−, NH
4
+
, NO
2
−
and NO
3
−
concentrations were determined in the soil extracts, and the same determinations plus ash weight, soluble carbohydrates,
proline, proteins andin vivo nitrate reductase in the plant roots and shoots.
Soil humidity decreased and salinity increased from March to August, with re-wetting occurring in late July. K+ and Cl− were much lower in the soils than Na+. Plant relative dry weight increased during summer due to the absorption of Na+ in addition to increased organic dry weight. The uptake of Na+ was not balanced by a similar uptake of Cl−.
Ammonium and nitrate decreased in soil and plants in parallel with increasing salinity. Nitrite was only found in the roots
and always in very low quantities. Proline was found only in March. The total soluble carbohydrates in the roots showed a
short increase in June when the sodium in the plants also increased. It was concluded that carbohydrates may be used to balance
osmotic shocks, but that another compatible compounds is necessary to maintatin long-term osmotic equilibrium.
The nitrate reductase activity, measuredin vivo, and the soluble protein changed roughly in parallel with the internal nitrate from May to August, suggesting that nitrogen
uptake and reduction in the plant is inhibited during summer when the soil is dry and very saline. This could be a direct
effect of drought and/or salinity on the plants, or an indirect onevia an inhibition of nitrifying bacteria. 相似文献
2.
Citrus Tristeza Virus (CTV), usually occurs in nature as a mixture of genotypes. Six naturally infected citrus
(Citrus sinensis) trees grafted on sour orange rootstock were collected from three citrus growing governorates
in Egypt (Sharqia, Qalyubia and Garbia). In this study, RT-PCR, Single-Strand Conformation Polymorphism
(SSCP) and nucleotide sequence analysis were used for four independent CTV genomic regions (p65, p18,
p20, and p23) to detect and assess the sequence and genetic variabilities among CTV Egyptian isolates. RTPCR products (650 bp) for the CTV p23 gene obtained from the selected isolates were used for the SSCP analysis
and DNA sequencing. SSCP patterns of p23 gene for individual isolates yielded different complex haplotype patterns. Nucleotide sequence analysis of p23 region amplified from six isolates under study revealed that p23 shared
high nucleotide identity 98.7% with T36 isolate from USA, Florida. Phylogenetic analysis of p23 gene indicated a
close evolutionary relationship between all examined isolates and Qaha isolate (T36 isolate group), suggesting that
they may have originated from closely related ancestors. Nucleotide sequence analysis of the three genes located
on CTV 3′-coterminal overhang, p18, p20 and p65, amplified from isolate A3, Sharqia governorate, revealed that
the p18, p65, and p20 genes were related to the T3-KB isolate from South Africa with 99%–100% sequence
homology. Phylogenetic relationship analysis for p65, p18 and p20 ORFs clustered the current A3 isolate with
T3 genotype group. The recombination analysis identified three of six isolates from Sharqia, and Garbia as potential recombinant for p23 gene. The isolates T36 and T3 were identified as major donors for recombination events
in isolate A3. Our results concluded that p23 ORF likely to be as a hotspot region for recombination and originated through recombination event. The current study indicated that recombination is an important factor for the
origin of CTV strains in Egypt. 相似文献
3.
Ming-Chi Wu Grace K. Arimura John S. Holcenberg Adel A. Yunis 《In vitro cellular & developmental biology. Plant》1982,18(9):750-754
Summary Cultured human pancreatic carcinoma cells (MIA PaCa-2) have been shown previously to be very sensitive toE. coli
l-asparaginase (EC II). The present studies have demonstrated that another enzyme,Acinetobacter glutaminase-asparaginase (AGA) is much more effective in inhibiting cell growth. At the concentration of 0.0025 U/ml of AGA
activity the enzyme totally inhibited cell growth, whereas the EC II with the same concentration did not show any effect.
The inhibition of cell growth correlated well with inhibition of protein and glycoprotein synthesis. The addition ofl-glutamine at the concentration of 1 mM completely reversed the inhibition of protein synthesis. Similarly, the addition ofl-glutamine at the concentration of 3 mM daily on 3 successive days after adding AGA resulted in significant reversal of growth inhibition. The results of this study
indicate that the action of AGA on MIA PaCa-2 is, to a great extent, exerted through itsl-glutaminase activity.
This work was supported in part by USPHS Grant CA 19182. Dr. Wu is recipient of Research Career Development Award Grant CA00686
and Dr. Yunis is a Howard Hughes Investigator. 相似文献
4.
5.
6.
Plant samples collected in Bahrain and data reported in the literature indicate the flora of Bahrain to contain 52 species (49 genera; 20 families) of medicinal interest. Of these plant species 20 appear to be indigenous and are being used in traditional herbal remedies for numerous afflictions. Preparation of such remedies appears to be simple and includes boiling, infusions, extraction of milled dry or fresh leaves, flowers, seeds or whole plants. Direct consumption of plant parts, raw or cooked, is also practiced. None of these plants has been studied systematically to evaluate their medicinal potential. 相似文献
7.
Pearce LR Huang X Boudeau J Pawłowski R Wullschleger S Deak M Ibrahim AF Gourlay R Magnuson MA Alessi DR 《The Biochemical journal》2007,405(3):513-522
The mTOR (mammalian target of rapamycin) protein kinase is an important regulator of cell growth. Two complexes of mTOR have been identified: complex 1, consisting of mTOR-Raptor (regulatory associated protein of mTOR)-mLST8 (termed mTORC1), and complex 2, comprising mTOR-Rictor (rapamycininsensitive companion of mTOR)-mLST8-Sin1 (termed mTORC2). mTORC1 phosphorylates the p70 ribosomal S6K (S6 kinase) at its hydrophobic motif (Thr389), whereas mTORC2 phosphorylates PKB (protein kinase B) at its hydrophobic motif (Ser473). In the present study, we report that widely expressed isoforms of unstudied proteins termed Protor-1 (protein observed with Rictor-1) and Protor-2 interact with Rictor and are components of mTORC2. We demonstrate that immunoprecipitation of Protor-1 or Protor-2 results in the co-immunoprecipitation of other mTORC2 subunits, but not Raptor, a specific component of mTORC1. We show that detergents such as Triton X-100 or n-octylglucoside dissociate mTOR and mLST8 from a complex of Protor-1, Sin1 and Rictor. We also provide evidence that Rictor regulates the expression of Protor-1, and that Protor-1 is not required for the assembly of other mTORC2 subunits into a complex. Protor-1 is a novel Rictor-binding subunit of mTORC2, but further work is required to establish its role. 相似文献
8.
Asha Thomas Georgia D. Tourassi Adel S. Elmaghraby Roland Valdes Jr. Saeed A. Jortani 《Clinical proteomics》2006,2(1-2):13-32
Data mining application to proteomic data from mass spectrometry has gained much interest in recent years. Advances made in proteomics and mass spectrometry have resulted in considerable amount of data that cannot be easily visualized or interpreted. Mass spectral proteomic datasets are typically high dimensional but with small sample size. Consequently, advanced artificial intelligence and machine learning algorithms are increasingly being used for knowledge discovery from such datasets. Their overall goal is to extract useful information that leads to the identification of protein biomarker candidates. Such biomarkers could potentially have diagnostic value as tools for early detection, diagnosis, and prognosis of many diseases. The purpose of this review is to focus on the current trends in mining mass spectral proteomic data. Special emphasis is placed on the critical steps involved in the analysis of surface-enhanced laser desorption/ionization mass spectrometry proteomic data. Examples are drawn from previously published studies and relevant data mining terminology and techniques are exlained. 相似文献
9.
The gene encoding the extracellular lipase of Staphylococcus xylosus (SXL) was cloned using PCR technique. The sequence corresponding to the mature lipase was subcloned in the pET-14b expression vector, with a strong T7 promoter, to construct a recombinant lipase protein containing six histidine residues at the N-terminal. High level expression of the lipase by Escherichia coli BL21 (DE3) cells harbouring the lipase gene containing expression vector was observed upon induction with 0.4 mM IPTG at 37 degrees C. One-step purification of the recombinant lipase was achieved with Ni-NTA resin. The specific activity of the purified His-tagged SXL was 1500 or 850 U/mg using tributyrin or olive oil emulsion as substrate, respectively. It has been proposed that the region near the residue Asp290 could be involved in the selection of the substrate. Therefore, we also mutated the residue Asp 290 by Ala using site-directed mutagenesis. The mutant SXL-D290A was overexpressed in E. coli BL21 (DE3) and purified with the same nickel metal affinity column. The specific activity of the purified His-tagged SXL-D290A mutant was 1000 U/mg using either tributyrin or olive oil emulsion as substrate. A comparative study of the wild type (His(6)-SXL) and the mutant (His(6)-SXL-D290A) proteins was carried out. Our results confirmed that Asp290 is important for the chain length specificity and catalytic efficiency of the enzyme. 相似文献
10.
Adel M. E. Attia Galal E. H. Elgemeie 《Nucleosides, nucleotides & nucleic acids》2013,32(6):1211-1218
Abstract A novel synthesis of 3-deazapyrimidine glycosides utilizing pyridine-2(1H)-ones or their sodium salts and α-halomonosugars namely D-glucose or D-galactose as starting components is described. 相似文献