نتایج جستجو برای: direct mutagenesis

تعداد نتایج: 451037  

Journal: :Systems microbiology and biomanufacturing 2022

As an important industrial enzyme, protease is widely used in feed, food and other fields. At present, the insufficient activity obtained from microorganisms cannot meet purpose of production. In this study, Bacillus amyloliquefaciens with high production was screened animal feces by plate transparent circle method. To improve protease, atmospheric room temperature plasma (ARTP) mutagenesis fir...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه مازندران - دانشکده علوم پایه 1391

یکی از علت های شکست و عدم موفقیت در تکنیک های کمک باروری(art) قطعه قطعه شدن dna اسپرم انسانی است، که ممکن است با انکوباسیون طولانی مدت اسپرم در دمای 37 درجه سانتی گراد به وجود آید. لذا در این مطالعه میزان قطعه قطعه شدن و آپوپتوز dna اسپرم انسانی بعد از آماده سازی به روش direct swim-up در زمان های مختلف انکوباسیون به وسیله تست scd و تکنیک tunel مورد ارزیابی قرار گرفت. در این مطالعه آینده نگر، ب...

Journal: :Cells 2021

The current SARS-CoV-2 pandemic underscores the importance of understanding evolution RNA genomes. While is subject to formation similar lesions as DNA, evolutionary and physiological impacts have on viral genomes are yet be characterized. Lesions that may drive can induce breaks repaired by recombination or cause base substitution mutagenesis, also known editing. Over past decade so, editing m...

Journal: :The Journal of Cell Biology 1989
S J Gould G A Keller N Hosken J Wilkinson S Subramani

The firefly luciferase protein contains a peroxisomal targeting signal at its extreme COOH terminus (Gould et al., 1987). Site-directed mutagenesis of the luciferase gene reveals that this peroxisomal targeting signal consists of the COOH-terminal three amino acids of the protein, serine-lysine-leucine. When this tripeptide is appended to the COOH terminus of a cytosolic protein (chloramphenico...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1982
L A Dodson R S Foote S Mitra W E Masker

An in vitro system in which bacteriophage T7 DNA is replicated and efficiently packaged into procapsids to form viable phage has been used to examine mutagenesis. The fidelity of replication was assayed both by measuring reversion of an amber mutation in an essential gene and by generation of temperature-sensitive mutants among the phage produced in vitro. Under standard reaction conditions, th...

2016
Summer B Thyme Laila Akhmetova Tessa G Montague Eivind Valen Alexander F Schier

The CRISPR/Cas system uses guide RNAs (gRNAs) to direct sequence-specific DNA cleavage. Not every gRNA elicits cleavage and the mechanisms that govern gRNA activity have not been resolved. Low activity could result from either failure to form a functional Cas9-gRNA complex or inability to recognize targets in vivo. Here we show that both phenomena influence Cas9 activity by comparing mutagenesi...

Journal: :BioTechniques 1998
A Siwkowski M Humphrey M B De-Young A Hampel

Random mutagenesis followed by an in vitro selection procedure was shown to be capable of identifying important bases of the hairpin ribozyme for cleavage of an RNA target sequence. The selection scheme enriched the RNA population for those molecules capable of efficient site-specific self-cleavage in the absence of ligation. Cleavable mutants were selected for all positions in loop 4 except fo...

Journal: :The EMBO journal 1999
Y Zhang Y M Altshuller S M Hammond F Hayes A J Morris M A Frohman

Activation of phosphatidylcholine-specific phospholipase D (PLD) constitutes an important part of the cellular response to agonist signaling. PLD1 is stimulated in vitro in a direct and synergistic manner by protein kinase C (PKC), ADP-ribosylation factor (ARF) and Rho family members. However, the direct and specific role of each of these effectors in agonist-stimulated PLD activation is poorly...

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