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Chap. 6B Enzymes Introduction to Enzymes How Enzymes Work
Chap. 6B Enzymes Introduction to Enzymes How Enzymes Work

... It is estimated that one-third of all proteins in a eukaryotic cell are phosphorylated, and one, or often many phosphorylation events are part of virtually every regulatory process. Some proteins have only one phosphorylation site, whereas others have several, and a few have dozens of sites for phos ...
Classification of Microorganisms
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...  DNA fingerprinting: Number and sizes of DNA fragments (fingerprints) produced by RE digests are used to determine genetic similarities.  Ribotyping: rRNA sequencing ...
Per cent of children with 1st cousin parents
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... a recessive disorder in which a person cannot process the amino acid phenylalanine. If the baby tests positive for phenylketonuria, the parents can put the baby on a phenylalanine-controlled diet. Such a diet is effective in preventing the mental disability that is characteristic of the untreated di ...
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Gene Tagging with Transposons

... • Transposable elements are stretches of DNA that can move to new locations in a genome • These elements can contain genes or be non-coding • Large portions of higher eukaryotes’ genomes are composed of either inert or active transposons (often as repetitive DNA) • Transposons are thus important evo ...
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... the relationship between DNA replication and induction of sporulation in a strain that does not require thymine for growth. In addition, we wanted to use a method which, unlike that of Mandelstam & Higgs (1974), did not rely on the imposition of synchrony on the cultures before resuspension in the s ...
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as PDF

... a blue light excitation source could be used. A blue excitable stain is therefore required for such cases. SYBR Green or Gel Green stains could serve for the purpose. Blue light is also convenient for visualization, because it is safe and also it passes through transparent plastic and glass. 1.4 Pre ...
PowerPoint file
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...  DNA fingerprinting: Number and sizes of DNA fragments (fingerprints) produced by RE digests are used to determine genetic similarities.  Ribotyping: rRNA sequencing  Polymerase chain reaction (PCR) can be used to amplify a small amount of microbial DNA in a sample. The Fig 10.14: Electrophoresis ...
CRACKING THE GENETIC CODE
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Chapter 3 sample - Scion Publishing

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... cDNA [1], the pig clone contained nucleotide sequences for 5' amino terminal signal peptide and complete sequence for a~-M/HI-30 mRNA and a large segment of 3' UT region. The sequence of the original clone (sti.1) was found to be identical to position 268-861 and 514-1107 of the two others (sti.l.4 ...
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... cleaves on the carboxyl side of basic side chains (Lys, Arg), whereas chymotrypsin cleaves on the carboxyl side of aromatics (Phe, Tyr, Trp) The active site consists of a “catalytic triad”: 1) Serine, to which the substrate binds 2) Histidine, which has the ability to donate and accept protons. 3) A ...
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Supporting Online Material

... Figure S1. Percentage of fluorescent cells upon transfection with normal (T pl.) or uracilsubstituted plasmids (U pl.). A Drosophila S2 cells, B HeLa cells. The number of observed fluorescent cells is also presented within the bars together with the total number of scored cells (shown in brackets). ...
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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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