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排序方式: 共有112条查询结果,搜索用时 15 毫秒
71.
Randa A Abusham RA Noor Zaliha Raja Rahman Abu Bakar Salleh Mahiran Basri 《Microbial cell factories》2009,8(1):20-9
Background
Many researchers have reported on the optimization of protease production; nevertheless, only a few have reported on the optimization of the production of organic solvent-tolerant proteases. Ironically, none has reported on thermostable organic solvent-tolerant protease to date. The aim of this study was to isolate the thermostable organic solvent-tolerant protease and identify the culture conditions which support its production. The bacteria of genus Bacillus are active producers of extra-cellular proteases, and the thermostability of enzyme production by Bacillus species has been well-studied by a number of researchers. In the present study, the Bacillus subtilis strain Rand was isolated from the contaminated soil found in Port Dickson, Malaysia. 相似文献72.
73.
GW Patton R Stephens IA Sidorov X Xiao RA Lempicki DS Dimitrov RH Shoemaker G Tudor 《BMC bioinformatics》2006,7(1):81
Background
Microarrays used for gene expression studies yield large amounts of data. The processing of such data typically leads to lists of differentially-regulated genes. A common terminal data analysis step is to map pathways of potentially interrelated genes. 相似文献74.
75.
Yvonne Welte James Adjaye Hans R Lehrach Christian RA Regenbrecht 《Cell communication and signaling : CCS》2010,8(1):1-10
Background
The fibroblast growth factor receptor (FGFR) interprets concentration gradients of FGF ligands and structural changes in the heparan sulfate (HS) co-receptor to generate different cellular responses. However, whether the FGFR generates different signals is not known.Results
We have previously shown in rat mammary fibroblasts that in cells deficient in sulfation, and so in HS co-receptor, FGF-2 can only stimulate a transient phosphorylation of p42/44MAPK and so cannot stimulate DNA synthesis. Here we demonstrate that this is because in the absence of HS, FGF-2 fails to stimulate the phosphorylation of the adaptor FGFR substrate 2 (FRS2). In cells possessing the HS co-receptor, FGF-2 elicits a bell-shaped dose response: optimal concentrations stimulate DNA synthesis, but supramaximal concentrations (≥ 100 ng/mL) have little effect. At optimal concentrations (300 pg/mL) FGF-2 stimulates a sustained dual phosphorylation of p42/44MAPK and tyrosine phosphorylation of FRS2. In contrast, 100 ng/mL FGF-2 only stimulates a transient early peak of p42/44MAPK phosphorylation and fails to stimulate appreciably the phosphorylation of FRS2 on tyrosine.Conclusions
These results suggest that the nature of the FGFR signal produced is determined by a combination of the HS co-receptor and the concentration of FGF ligand. Both the phosphorylation of the adaptor FRS2, the kinetics (sustained or transient) of phosphorylation of p42/44(MAPK) are varied, and so differing cellular responses are produced. 相似文献76.
77.
78.
79.
The phylogenetic origin of the bifunctional tyrosine-pathway protein in the enteric lineage of bacteria 总被引:5,自引:0,他引:5
Because bifunctional enzymes are distinctive and highly conserved products
of relatively infrequent gene-fusion events, they are particularly useful
markers to identify clusters of organisms at different hierarchical levels
of a phylogenetic tree. Within the subdivision of gram-negative bacteria
known as superfamily B, there are two distinctive types of tyrosine-pathway
dehydrogenases: (1) a broad- specificity dehydrogenase (recently termed
cyclohexadienyl dehydrogenase [CDH]) that can utilize either prephenate or
L-arogenate as alternative substrates and (2) a bifunctional CDH that also
posseses chorismate mutase activity. (T-proteins). The bifunctional
T-protein, thought to be encoded by fused ancestral genes for chorismate
mutase and CDH, was found to be present in enteric bacteria (Escherichia,
Shigella, Salmonella, Citrobacter, Klebsiella, Erwinia, Serratia,
Morganella, Cedecea, Kluyvera, Hafnia, Edwardsiella, Yersinia, and Proteus)
and in Aeromonas and Alteromonas. Outside of the latter "enteric lineage,"
the T-protein is absent in other major superfamily-B genera, such as
Pseudomonas (rRNA homology group I), Xanthomonas, Acinetobacter, and
Oceanospirillum. Hence, the T-protein must have evolved after the
divergence of the enteric and Oceanospirillum lineages.
3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase-phe, an early-pathway
isozyme sensitive to feedback inhibition by L- phenylalanine, has been
found in each member of the enteric lineage examined. The absence of both
the T-protein and DAHP synthase-phe elsewhere in superfamily B indicates
the emergence of these character states at approximately the same
evolutionary time.
相似文献
80.
Biotinyl-oligosaccharides are a relatively new generation of saccharide
probes that enable immobilization of desired oligosaccharides on
streptavidin matrices for studies of carbohydrate-protein interactions.
Here we describe the facile preparation of biotinyl-l-3-(2-naphthyl)-
alanine hydrazide (BNAH) derivatives of oligosaccharides, containing a
strong UV absorbing and fluorescent group, in which the ring of the
reducing-end monosaccharide is nonreduced. We evaluate reactivities of
immobilized BNAH- N -glycans with plant lectins that recognize aspects of
the oligosaccharide core or outer-arms. We make some comparisons with
2-amino-6-amidobiotinyl-pyridine (BAP) derivatives obtained by reductive
amination, and 6-(biotinyl)-aminocaproyl-hydrazide (BACH) derivatives which
have a longer spacer-arm. N -Glycan-BNAH and-BAP derivatives have, overall,
comparable reactivities with lectins which recognize N -glycan outer-arms
or the trimannosyl core, but only BNAH and BACH derivatives are bound by
lectins which recognize the non- reduced core. Moreover, with Pisum sativum
agglutinin (PSA) which additionally requires the fucosyl- N-
glycan-asparaginyl core for high affinity binding, the immobilized BNAH
derivative (which is an alanine hydrazide beta-glycoside) can substitute
for the natural beta- glycosylasparaginyl core, whereas the BACH derivative
(aminocaproyl- hydrazide-beta-glycoside) is less effective. BNAH is a
derivatization reagent of choice, therefore, for solid phase
carbohydrate-binding experiments with immobilized N -glycans.
相似文献