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Terpene Biosynthesis
Terpene Biosynthesis

Plant aromatic amino acid decarboxylases
Plant aromatic amino acid decarboxylases

... categories remain almost identical. Due to this high sequence homology, it has historically been difficult to predict the function of any given plant AAAD through sequence comparison. This extensive homology has lead to a major problem in distinguishing activity and substrate specificity from a prim ...
An Introduction to Enzyme Science
An Introduction to Enzyme Science

... the enzyme of interest from other contaminants (e.g., proteins, solutes, etc.) affecting the enzyme’s activity. In practice, absolute purity is not required as long as other contaminating enzymes and proteins are without effect on the enzyme of interest. It is helpful to apply the principles of orga ...
risk and technical assessment report
risk and technical assessment report

... were no concerns with the safety of B. circulans, when used as a source of β-galactosidase. Question 2: What is the risk to the public from the use of β-galactosidase derived from B. circulans as a processing aid? No safety concerns with the use of this enzyme as a processing aid were raised. The sa ...
FLAVIN MONONUCLEOTIDE PHOSPHATASE FROM GOAT LIVER: A POSSIBLE TARGET FOR
FLAVIN MONONUCLEOTIDE PHOSPHATASE FROM GOAT LIVER: A POSSIBLE TARGET FOR

Glucose metabolism in Trypanosoma cruzi
Glucose metabolism in Trypanosoma cruzi

Taxonomic characterization of Ochrobactrum sp. isolates from soil
Taxonomic characterization of Ochrobactrum sp. isolates from soil

... cluster, a separate DNA–DNA reassociation group and showed, as a biological particularity, a strict preference for the rhizoplane as habitat. Diagnostic phenotypic characters were found. This indicated that REP group J strains represent a further new species, although phylogenetic analyses using 16S ...
Autotrophic CO2 fixation via the reductive tricarboxylic acid cycle in
Autotrophic CO2 fixation via the reductive tricarboxylic acid cycle in

... to have been among the first types of organisms on Earth (e.g. Huber and Wächtershäuser, 1997; Russell and Hall, 1997). Phylogenetic analyses based on 16S rRNA and whole genomes place autotrophic hyperthermophiles at the base of the evolutionary tree of life, lending evidence to the hypothesis that ...
Physiological and Chemical Properties of a
Physiological and Chemical Properties of a

... An inorganic pyrophosphatase was purified from Desulfuvibrio desulfuricans strain BERRE SOL. Its activity was increased up to 130-fold by reduction with reagents (Na2S20,, Na[BH,], Na,S, etc.) of Ei values less than -0.14V at pH 7.0 and 25'. The pure enzyme was isoelectric at pH 6.55 ;its molecular ...
Enzyme Mechanisms - Weber State University
Enzyme Mechanisms - Weber State University

Bacterial methionine biosynthesis
Bacterial methionine biosynthesis

... Methionine is essential in all organisms, as it is both a proteinogenic amino acid and a component of the cofactor, S-adenosyl methionine. The metabolic pathway for its biosynthesis has been extensively characterized in Escherichia coli; however, it is becoming apparent that most bacterial species d ...
Fibrinogen Bern I: Substitution y 337 Asn + Lys Is
Fibrinogen Bern I: Substitution y 337 Asn + Lys Is

... functional defect caused by structural alteration in the fibrinogen molecule. Most dysfibrinogenemias have thus far been detected by virtue of a prolonged thrombin clotting time and, therefore, mainly represent variants with defective fibrinogen to fibrin conversion. More than 240 abnormal fibrinoge ...
New peptide and gene coding for same
New peptide and gene coding for same

... RNA were extracted from human atrium cordis by a method disclosed in Chirgwin (Chirgwin, J. M. et. al., Biochemistry 18, 5294-5299, 1979), and enriched for poly (A)+ RNA (mRNA) with an oligo (dT) cellulose column. The poly (A) RNA were used to prepare a cDNA library according to the Okayama-Berg met ...
41 Purine and Pyrimidine Metabolism
41 Purine and Pyrimidine Metabolism

... respectively. A primary site of regulation is the synthesis of PRPP. PRPP synthetase is negatively affected by GDP and, at a distinct allosteric site, by ADP. Thus, the simultaneous binding of an oxypurine (eg., GDP) and an aminopurine (eg., ADP) can occur with the result being a synergistic inhibit ...
File
File

... molecular level. The application of new experimental techniques for the isolation and manipulation of specific fragments of DNA has greatly increased our understanding of the processes responsible for the replication and expression of genetic information. Furthermore, the ability to isolate a specif ...
Kinetic studies of human tyrosyl
Kinetic studies of human tyrosyl

... enzyme that relaxes DNA supercoiling and relieves torsional strain of DNA during replication, repair and transcription processes by making single stranded breaks on DNA, unwinding and religating the DNA ends in the cleaved strand [1]. During the process, DNA becomes covalently linked to Topo I via t ...
Diiffusional correlations among multiple active sites in a single enzyme
Diiffusional correlations among multiple active sites in a single enzyme

... modification of the model where the enzyme–substrate interactions are removed, while still retaining binding interactions with the active site beads. The plots of g R(r) and g P(r) for this case are given in Fig. 5 and the lack of structure is evident. For this model the substrate molecules can free ...
BIOCHEMISTRY AND MOLECULAR BIOLOGY Problem Unit Two
BIOCHEMISTRY AND MOLECULAR BIOLOGY Problem Unit Two

... inhibitor (i.e., a bacterial toxin, a chemical, etc.), the overproduction of an enzyme, or the introduction of a foreign enzyme (i.e., viral infection). Enzymes are popular therapeutic targets. Pharmaceuticals are frequently enzyme inhibitors. Enzyme assays are important in diagnosis. A diminution o ...
Characterization of the chimeric seven
Characterization of the chimeric seven

... pump that has been found in a variety of marine bacteria. Recently, many PR-like genes were found in non-marine environments. The goal of this study is to explore the function of rhodopsins that exist only as partial proteoopsin genes using chimeras with marine green PR (GPR). We isolated nine parti ...
Enzyme Mechanisms
Enzyme Mechanisms

18. enzymes iii
18. enzymes iii

... Frederick August Kekule (LT, 1829-1867), master of structural chemistry. After receiving his doctoral degree from the University of Strasbourg in 1874, he taught at the Universities of Erlangen and Wurzburg, eventually becoming Professor of Chemistry at the University of Berlin in 1892 while succeed ...
Enzyme Mechanisms
Enzyme Mechanisms

Chondroitinase ABC I from Proteus vulgaris: cloning, recombinant
Chondroitinase ABC I from Proteus vulgaris: cloning, recombinant

... GalAG, galactosaminoglycan; GalNAc, N -acetylgalactosamine; IdoA, iduronic acid; UA, 4,5 unsaturated uronic acid. ...
Nucleotide Metabolism - Oregon State University
Nucleotide Metabolism - Oregon State University

Nucleotide Metabolism
Nucleotide Metabolism

... OMP Decarboxylase is one of the Most Efficient Enzymes Known and Makes UMP CTP is Synthesized from UTP by CTP Synthetase CTP Synthetase Activated by GTP, Inhibited by CTP and Phosphorylation CTP Synthetase Helps to Balance Purines and Pyrimidines ...
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Restriction enzyme

A restriction enzyme or restriction endonuclease is an enzyme that cuts DNA at or near specific recognition nucleotide sequences known as restriction sites. Restriction enzymes are commonly classified into three types, which differ in their structure and whether they cut their DNA substrate at their recognition site, or if the recognition and cleavage sites are separate from one another. To cut DNA, all restriction enzymes make two incisions, once through each sugar-phosphate backbone (i.e. each strand) of the DNA double helix.These enzymes are found in bacteria and archaea and provide a defense mechanism against invading viruses. Inside a prokaryote, the restriction enzymes selectively cut up foreign DNA in a process called restriction; while host DNA is protected by a modification enzyme (a methyltransferase) that modifies the prokaryotic DNA and blocks cleavage. Together, these two processes form the restriction modification system.Over 3000 restriction enzymes have been studied in detail, and more than 600 of these are available commercially. These enzymes are routinely used for DNA modification in laboratories, and are a vital tool in molecular cloning.
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