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Rich Region (rich + region)
Selected AbstractsSequence and organization of the mitochondrial genome of the Chagas disease vector, Triatoma dimidiataINSECT MOLECULAR BIOLOGY, Issue 3 2001E. M. Dotson Abstract The 17 019 bp mitochondrial genome of Triatoma dimidiata is composed of thirteen protein coding sequences, twenty-two tRNAs, small and large ribosomal units, and a control region. The gene order and orientation are identical to that of Drosophila yakuba. The nucleotide composition is biased toward adenine and thymine (69.5% A + T). The 2.1 kb putative control region, known as the A + T rich region in most insects, has an A + T bias of 66%, but contains a 400 bp sequence that is 77.5% A + T and two other distinct regions: (1) one with a lower A + T bias (60.1%) and (2) a region of eight tandem repeat units. The identified 1.4 kb nuclear copy of mitochondrial sequences encompasses the string of Gs and the beginning of the cytochrome c oxidase 1 gene but lacks the 1.8 kb region spanning the eight tandem repeats and the 5, end of the NADH dehydrogenase subunit II gene. [source] Studies on glass transition temperature of mono and bilayer protein films plasticized by glycerol and olive oilJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Babak Ghanbarzadeh Abstract Thermomechanical and thermal properties of whey protein, maize prolamin protein (zein), and the laminated whey protein,zein films were studied. The dynamic mechanical (thermal) analysis (DMTA) results showed that the single zein film had higher Tg than single whey protein and zein,whey laminated films. The shift in the Tg values of films from 31.2°C in whey protein film and 88.5°C in the zein film to 82.8°C in the laminated whey protein,zein films may be implied some interaction formation between the two polymers. The small tan , peaks were observed at ,50°C in zein,glycerol films and at ,22.37°C in the whey protein films and can be related to ,-relaxation phenomena or presence of glycerol rich region in polymer matrix. Zein-olive oil and zein,whey protein,olive oil films showed tan , peaks corresponded the Tg values at 113.8, and 92.4°C, respectively. Thus, replacing of glycerol with olive oil in film composition increased Tg. A good correspondence was obtained when DSC results were compared with the tan , peaks in DMTA measurements. DSC thermograms suggested that plasticizers and biopolymers remained a homogeneous material throughout the cooling and heating cycle. The results showed that Tg of zein,glycerol films predicted by Couchman and Karasz equation is very close to value obtained by DSC experiments. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] {111} Twin Formation and Abnormal Grain Growth in Barium Strontium TitanateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2003Byoung-Ki Lee Two series of experiments were performed to study the experimental conditions for the formation of {111} twins and related microstructures in barium strontium titanate ((Ba, Sr)TiO3). In the first series, the phase equilibria in the BaTiO3,SrTiO3,TiO2 system were determined. XRD and WDS analysis, done in the BaTiO3 -rich region, of 45(Ba,Sr)TiO3,10TiO2 samples annealed at 1250°C for 200 h in air showed that (Ba,Sr)TiO3 was in equilibrium with Ba6Ti17O40 (B6T17) and Ba4Ti13O30 phases with strontium solubility (Sr/(Ba + Sr)) of ,0.02 and 0.20, respectively. In the second series the microstructures of samples consisting of a mixture of (Ba,Sr)TiO3 and 2.0 mol% TiO2, were observed after sintering at 1250°C for 100 h in air. {111} twins formed only in the samples with faceted B6T17 second phase particles, similar to the case of BaTiO3. In these samples, abnormal grain growth occurred in the presence of the {111} twins. In contrast, no {111} twins formed and no abnormal grain growth occurred in the samples containing second phase particles other than B6T17. With an increased substitution of strontium for barium, the aspect ratio of abnormal grains containing {111} twin lamellae was reduced. This result was attributed to a reduction in the relative stability of the {111} planes with the strontium substitution. [source] The galactokinase of Hypocrea jecorina is essential for cellulase induction by lactose but dispensable for growth on d -galactoseMOLECULAR MICROBIOLOGY, Issue 4 2004Bernhard Seiboth Summary Lactose is the only soluble carbon source which can be used economically for the production of cellulases or heterologous proteins under cellulase expression signals by Hypocrea jecorina (=Trichoderma reesei). Towards an understanding of lactose metabolism and its role in cellulase formation, we have cloned and characterized the gal1 (galactokinase) gene of H. jecorina, which catalyses the first step in d -galactose catabolism. It exhibits a calculated Mr of 57 kDa, and shows moderate identity (about 40%) to its putative homologues of Saccharomyces cerevisiae and Kluyveromyces lactis. Gal1 is a member of the GHMP family, shows conservation of a Gly/Ser rich region involved in ATP binding and of amino acids (Arg 51, Glu 57, Asp 60, Asp 214, Tyr 270) responsible for galactose binding. A single transcript was formed constitutively during the rapid growth phase on all carbon sources investigated and accumulated to about twice this level during growth on d -galactose, l -arabinose and their corresponding polyols. Deletion of gal1 reduces growth on d -galactose but does only slightly affect growth on lactose. This is the result of the operation of a second pathway for d -galactose catabolism, which involves galactitol as an intermediate, and whose transient concentration is strongly enhanced in the delta- gal1 strain. In this pathway, galactitol is catabolised by the lad1 -encoded l -arabinitol-4-dehydrogenase, because a gal1/lad1 double delta-mutant failed to grow on d -galactose. In the delta- gal1 strain, induction of the Leloir pathway gene gal7 (encoding galactose-1-phosphate uridylyltransferase) by d -galactose, but not by l -arabinose, is impaired. Induction of cellulase gene expression by lactose is also impaired in a gal1 deleted strain, whereas their induction by sophorose (the putative cellulose-derived inducer) was shown to be normal, thus demonstrating that galactokinase is a key enzyme for cellulase induction during growth on lactose, and that induction by lactose and sophorose involves different mechanisms. [source] | |||||||||||||