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901.
Romeu Cardoso Guimarães 《Origins of life and evolution of the biosphere》2011,41(4):357-371
An investigation of the biosynthesis pathways producing glycine and serine was necessary to clarify an apparent inconsistency
between the self-referential model (SRM) for the formation of the genetic code and the model of coevolution of encodings and
of amino acid biosynthesis routes. According to the SRM proposal, glycine was the first amino acid encoded, followed by serine.
The coevolution model does not state precisely which the first encodings were, only presenting a list of about ten early assignments
including the derivation of glycine from serine—this being derived from the glycolysis intermediate glycerate, which reverses
the order proposed by the self-referential model. Our search identified the glycine-serine pathway of syntheses based on one-carbon
sources, involving activities of the glycine decarboxylase complex and its associated serine hydroxymethyltransferase, which
is consistent with the order proposed by the self-referential model and supports its rationale for the origin of the genetic
code: protein synthesis was developed inside an early metabolic system, serving the function of a sink of amino acids; the
first peptides were glycine-rich and fit for the function of building the early ribonucleoproteins; glycine consumption in
proteins drove the fixation of the glycine-serine pathway. 相似文献
902.
Joseph A. Marsh 《Journal of molecular biology》2009,391(2):359-318
Obtaining detailed structural models of disordered states of proteins under nondenaturing conditions is important for a better understanding of both functional intrinsically disordered proteins and unfolded states of folded proteins. Extensive experimental characterization of the drk N-terminal SH3 domain unfolded state has shown that, although it appears to be highly disordered, it possesses significant nonrandom secondary and tertiary structure. In our previous attempts to generate structural models of the unfolded state using the program ENSEMBLE, we were limited by insufficient experimental restraints and conformational sampling. In this study, we have vastly expanded our experimental restraint set to include 1H-15N residual dipolar couplings, small-angle X-ray scattering measurements, nitroxide paramagnetic relaxation enhancements, O2-induced 13C paramagnetic shifts, hydrogen-exchange protection factors, and 15N R2 data, in addition to the previously used nuclear Overhauser effects, amino terminal Cu2+-Ni2+ binding paramagnetic relaxation enhancements, J-couplings, chemical shifts, hydrodynamic radius, and solvent accessibility restraints. We have also implemented a new ensemble calculation methodology that uses iterative conformational sampling and seeks to calculate the simplest possible ensemble models. As a result, we can now generate ensembles that are consistent with much larger experimental data sets than was previously possible. Although highly heterogeneous and having broad molecular size distributions, the calculated drk N-terminal SH3 domain unfolded-state ensembles have very different properties than expected for random or statistical coils and possess significant nonnative α-helical structure and both native-like and nonnative tertiary structure. 相似文献
903.
904.
905.
This review focuses on utilization of plant lectins as medical diagnostic reagents and tools. The lectin-related diagnostic
is aimed at detection of several diseases connected to alteration of the glycosylation profiles of cells and at identification
of microbial and viral agents in clinical microbiology. Certain lectins, proposed for or used as diagnostic tools could even
recognize those cellular determinants, which are not detected by available antibodies. Broad information is presented on the
lectinomics field, illustrating that lectin diagnostics might become practical alternative to antibody-based diagnostic products.
In addition, the rising trend of lectin utilization in biomedical diagnostics might initiate a development of innovative methods
based on better analytical technologies. Lectin microarray, a rapid and simple methodology, can be viewed as an example for
such initiative. This technology could provide simple and efficient screening tools for analysis of glycosylation patterns
in biological samples (cellular extracts, tissues and the whole cells), allowing thus personalized detection of changes associated
with carbohydrate-related diseases. 相似文献
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909.
O. Modesto Olanya Joseph E. Sites Aaron K. Hoshide 《Biocontrol Science and Technology》2016,26(5):651-664
Published research on process-based models for biocontrol of foodborne pathogens on produce is limited. The aim of this research was to develop cost model estimates for competitive exclusion (CE) process using Pseudomonas fluorescens and Pseudomonas chlororaphis (non-plant pathogenic and non-human pathogen) as biocontrol against Salmonella enterica on tomatoes. Cost estimates were based on material inputs, equipment, facilities, and projected processing conditions of post-harvest packaging of tomatoes. The microbiological data for inactivation of S. enterica was based on published papers. The small-scale processing facility was assumed to have a processing capacity of 2000 kg of tomatoes/hour for 16 h per day, operational 6 days a week, and for 3-months /year. The large-scale facility was assumed to have a processing capacity of 100,000 kg of tomatoes/hour. Estimated initial capital investment costs for small and large-scale models (production facility) were US$391,000 and US$2.1 million. Application of CE for biocontrol of S. enterica on tomatoes was estimated at US$0.0058–0.073/kg of tomatoes during commercial processing operations. This exceeds chlorine wash technology estimated at US$0.00046/kg and is competitive with gaseous chlorine dioxide at US$0.02–0.21/kg. For high-value produce, CE may complement existing technologies increase food safety, reduce storage loses, and extend shelf life of produce. 相似文献
910.