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The nature of mycelial lipolytic enzymes in filamentous fungi
The nature of mycelial lipolytic enzymes in filamentous fungi

... was first reported by Dawson in 1958 [6]. It is of course recognised that the phospholipase B type of activity could be due to the action of phospholipase A1 and highly active lysophospholipase. No evidence for the presence of phospholipase A2 was found associated with any of the organism examined. ...
Enzyme Kinetics and Mechanisms
Enzyme Kinetics and Mechanisms

... hydrolysis is dependent only on the substrate, and therefore proceeds with a First Order Rate Constant of 839 min-1. 5. Rate constants of different order cannot be compared. However, the ratio of the first order rate constant to the second order rate constant gives an effective Molarity. 6. In order ...
14-31 - McGraw Hill Higher Education
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Fibrinogen Bern I: Substitution y 337 Asn + Lys Is
Fibrinogen Bern I: Substitution y 337 Asn + Lys Is

... sequence analysis of exon VI11 showed the presence of two bands at the same migration distance, corresponding to Lys (AAC + AAA). amino acid substitution y 337 Asn The purified double-stranded PCR-derived fragment was cloned and subjected to sequence analysis. Normal and mutated alleles of fibrinoge ...
Application Note - Greiner Bio-One
Application Note - Greiner Bio-One

Microplate-Based Pathlength Correction Method for Photometric
Microplate-Based Pathlength Correction Method for Photometric

... Another limitation is that other than water, there must not be any other assay component that absorbs light at 900–975 nm area. In addition, pathlength correction cannot be used in turbidometric assays where light scattering from solid particles is measured. The particles cause some scattering at th ...
6_Enzymes - WordPress.com
6_Enzymes - WordPress.com

... Natural protection: Sugarcane tops contain invertase, which reduces the sugar % from sugarcane. So the sugarcane tops are removed at the time of harvest to remove the invertase. Thus the sugar % can be increased. Specificity of the enzymes One of the characteristic feature which distinguishes enzyme ...
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Application Note 129 – Eppendorf MixMate

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... amino acid #797-804 for human red blood cell plasma membrane Ca2+pumps [38], was used to design the 5 ’ forward primer 5’AC(A/T)GATGGATCCAATGATGGACCAGC(T/A)TTAAA3‘. The reverse 3’ primer S’ATCCTCGAGCAAATTAACCCA(T/C)AACAT’ITAAC3’ was based on VQMLWVNL, found at amino acids #885-895 for human red bloo ...
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... destined to be modified in a glutamine codon (CAG). (b) Further transcription unveils the intronic editing site complementary sequence (ECS), which somehow base-pairs and forms a helix with the coding region, looping out intervening sequences. Exonic sequences are in green, and intronic sequences ar ...
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... same mutation by using a single, large culture, as described in Methods. The numerous colonies isolated from this culture on succinate medium containing ally1 alcohol were re-isolated on the same medium. Five per cent retained their ability to grow on methanol medium. Among 1400 colonies unable to g ...
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PopGen 8: Transient verses equilibrium polymorphism Mutation

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... From the Author With the pace of current research, the biological sciences change incredibly fast, particularly in the fields of molecular genetics, specifically gene expression. Therefore, as a veteran biology teacher, I am constantly looking for resources that include up-to-date research, prompt ...
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... The TREX complex contains THO and 2 mRNA export factors • Human TREX contains Aly/REF, UAP56, and the human counterpart of the yeast THO complex. The human THO complex only associates with spliced mRNA and not with unspliced pre-mRNA. • Recent data indicate that recruitment of the human TREX comple ...
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Genetics of Arabidopsis thaliana

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Chapter 12

... • Mutations in the promoter are uninducible and cis-acting. • When mutant and wild-type subunits are present, a single lacI–d mutant subunit can inactivate a tetramer whose other subunits are wild-type. • lacI–d mutations occur in the DNA-binding site. – Their effect is explained by the fact that re ...
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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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