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P site - Industrial ISD
P site - Industrial ISD

... pair of complimentary nucleotides with another nucleotide pair is called a base-pair substitution. • Some base-pair substitutions have little or no impact on protein function. • In silent mutations, alterations of nucleotides still indicate the same amino acids because of redundancy in the genetic c ...
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... JAK2 is an essential protein in erythropoiesis and myeloid differentiation. Mutations in JAK2 affect its structure and function in the JAK-STAT pathway, leading to myeloproliferative diseases. The production of inactive and soluble proteins has shown to be a difficult task. In this study, bac-to-bac ...
Biochemical Testing of Macromolecules
Biochemical Testing of Macromolecules

... or when two or more sections of the chain lie next to each other and fold into beta () pleaded sheets. Tertiary structure forms when the chain with its alpha helices and beta pleaded sheets fold back on itself. This structure is then held together by a variety of hydrogen bonds, ionic bonds, disulf ...
A group of interacting yeast DNA replication genes.
A group of interacting yeast DNA replication genes.

... suppressor of two cold-sensitive mutations, cdc45 and cdc54, we investigated its genetic interactions with the other members of this group. The results of this analysis are summarized in Figure 1, which shows instances of both synthetic lethality as well as suppression. We take up the evidence for e ...
Unit 28: Understand the Principles of Inheritance and
Unit 28: Understand the Principles of Inheritance and

... P8 requires learners to use the Hardy-Weinberg Principle to explain how evolution occurs, with an example population analysed by applying the Hardy-Weinberg equation. Suitable evidence would be a poster or report. This may be assessed at the same time as P6. P9 requires learners to describe genetic ...
Inquiry into Life Twelfth Edition
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GENE MUTATIONS - The Open Door Web Site : Home Page
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Evolutionary dynamics of RNA-like replicator systems

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Enzymes
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The Depth of Chemical Time and the Power of Enzymes
The Depth of Chemical Time and the Power of Enzymes

... Why would one wish to know the rate of a biological reaction in the absence of an enzyme? That information would allow biologists to appreciate what natural selection has accomplished in the evolution of enzymes as proficient catalysts and would enable chemists to compare enzymes with artificial cat ...
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The Depth of Chemical Time and the Power of Enzymes as Catalysts
The Depth of Chemical Time and the Power of Enzymes as Catalysts

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A novel species of thermoacidophilic archaeon, Sulfolobus
A novel species of thermoacidophilic archaeon, Sulfolobus

... presence of each sugar or amino acid at a concentration of 0.1 YO.In order to test for autotrophic growth on sulfurcontaining inorganic compounds, washed cells were placed in flasks containing modified Allen's medium without any organic compounds, but with specific sulfur compounds in suspension (0. ...
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... from a combinatorial library by the phage display approach was composed of just five amino acid residues: Ala, Gly, Glu, Lys, and Ile (4). In the cases of the 53-residue Arc repressor (5) and the 58-residue bovine pancreatic trypsin inhibitor (6), multiple alanine substitutions were made, and the pr ...
CH_16_5_16_6_Enzymes_Enzyme_Action
CH_16_5_16_6_Enzymes_Enzyme_Action

... Copyright © 2012 by Pearson Education, Inc. ...
Amino Acids, Proteins, and Enzymes
Amino Acids, Proteins, and Enzymes

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Chapter 5 - macromolecules

... a polynucleotide • Adjacent nucleotides are joined by covalent bonds that form between the —OH group on the 3 carbon of one nucleotide and the phosphate on the 5 carbon on the next abc…lmnop • sugar-phosphate backbone (side of ladder) with nitrogenous bases as rungs of ladder • The sequence of bas ...
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Studying copy number variations using a nanofluidic platform

... Copy number variations (CNVs) in the human genome are conventionally detected using highthroughput scanning technologies, such as comparative genomic hybridization and high-density single nucleotide polymorphism (SNP) microarrays, or relatively low-throughput techniques, such as quantitative polymer ...
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11.7 Repressor binds cooperatively at each operator using a helix

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... Mitochondrial oxygen consumption was measured polarographically at 37 °C using a respiratory system (System S 200A, Strathkelvin Instruments, Glasgow, Scotland). Mitochondria (2 mg protein/ml) were suspended in respiration buffer (130 mmol/L KCl, 5 mmol/L K2HPO4, 20 mmol/L MOPS, 2.5 mmol/L EGTA, 1 μ ...
Index case of acute myeloid leukemia in a family
Index case of acute myeloid leukemia in a family

... postulated that it was a germ line mutation. We confirmed this by conducting Sanger sequencing of the CEBPA gene in genomic DNA isolated from skin fibroblasts (Figure 1A). This is a nonsense mutation located downstream of the p30 start codon (Figure 1B), and thus unique from the majority of previous ...
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Deoxyribozyme



Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of catalyzing specific chemical reactions, similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,there are no known naturally occurring deoxyribozymes.Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that selectively bind a target ligand, but do not catalyze a subsequent chemical reaction.With the exception of ribozymes, nucleic acid molecules within cells primarily serve as storage of genetic information due to its ability to form complementary base pairs, which allows for high-fidelity copying and transfer of genetic information. In contrast, nucleic acid molecules are more limited in their catalytic ability, in comparison to protein enzymes, to just three types of interactions: hydrogen bonding, pi stacking, and metal-ion coordination. This is due to the limited number of functional groups of the nucleic acid monomers: while proteins are built from up to twenty different amino acids with various functional groups, nucleic acids are built from just four chemically similar nucleobases. In addition, DNA lacks the 2'-hydroxyl group found in RNA which limits the catalytic competency of deoxyribozymes even in comparison to ribozymes.In addition to the inherent inferiority of DNA catalytic activity, the apparent lack of naturally occurring deoxyribozymes may also be due to the primarily double-stranded conformation of DNA in biological systems which would limit its physical flexibility and ability to form tertiary structures, and so would drastically limit the ability of double-stranded DNA to act as a catalyst; though there are a few known instances of biological single-stranded DNA such as multicopy single-stranded DNA (msDNA), certain viral genomes, and the replication fork formed during DNA replication. Further structural differences between DNA and RNA may also play a role in the lack of biological deoxyribozymes, such as the additional methyl group of the DNA base thymidine compared to the RNA base uracil or the tendency of DNA to adopt the B-form helix while RNA tends to adopt the A-form helix. However, it has also been shown that DNA can form structures that RNA cannot, which suggests that, though there are differences in structures that each can form, neither is inherently more or less catalytic due to their possible structural motifs.
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