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2012 HSC Biology Marking Guidelines
2012 HSC Biology Marking Guidelines

... Criteria • Provides an in-depth understanding of germ line mutation and reasons for its impact on whole organism phenotypes – transmitted to offspring – all cells of offspring contain mutation • Provides an in-depth understanding of transposons in their disruption of genes in genomes – insertion des ...
Genetic Engineering of Field, Industrial and Pharmaceutical Crops
Genetic Engineering of Field, Industrial and Pharmaceutical Crops

... netic makeup by manipulating the genome—either by introduction, deletion, substitution, or silencing of an individual gene or group of genes of interest. The functionality of transgenes has expanded with time. In the beginning, only traits that exhibited complete dominance, free of the interaction f ...
Recycling of vitamin B12 and NAD+ within the Pdu
Recycling of vitamin B12 and NAD+ within the Pdu

... products (56). The extract was the first workable treatment for the disease. These events in turn led to discovery of the water soluble vitamin, called vitamin B12, in the liver juice in 1948 by Karl A. Folkers (181) and E. Lester Smith (212). In 1955, the B12 structure was elucidated by X-ray cryst ...
Two Classes of sir3 Mutants Enhance the sir1
Two Classes of sir3 Mutants Enhance the sir1

... plasmids that rescued the sir3-eso mutants were made by introducing pJR273, digested with BamHI and ClaI, into strains LPY238 and LPY222 for pLP465 and pLP468, respectively; and from pLP187, digested with ClaI and StuI, into strains LPY275 and JRY188 for pLP464 and pLP675, or with StuI and NruI, int ...
BIO 402 - National Open University of Nigeria
BIO 402 - National Open University of Nigeria

... London, in 1665 described cork and other cells and introduced the term cell. H is was the first drawing ever made of cells. Microscopes at that time magnified 100 to 200 times with a distortion of shape and color that increased with magnification. Nevertheless, these microscopes revealed many new th ...
Cholesterol Synthesis
Cholesterol Synthesis

... acids, eicosanoids, retinoids, & various non-polar xenobiotics (drugs & other foreign compounds). Some P450 enzymes have broad substrate specificity.  Mechanisms for detoxification of non-polar compounds include reactions such as hydroxylations that increase polarity, so that the products of these ...
Electrophoretic karyotypes of clinically isolated yeasts
Electrophoretic karyotypes of clinically isolated yeasts

... The electrophoretic karyotypes of the 78 C. albicans isolates were compared with that of a standard strain (FC18) under conditions (Fig la) in which their chromosomes were well separated over the entire size range in a single gel, and also under conditions (Fig. 1b) in which chromosomes smaller than ...
Bioinformatics - cs@union
Bioinformatics - cs@union

... …conceptualizing biology in terms of molecules (in the sense of physical chemistry) and applying “informatics techniques” (derived from disciplines such as applied maths, computer science and statistics) to understand and organize the information associated with these molecules, on a large scale. In ...
Increased activity of 16-membered lactone ring macrolides against
Increased activity of 16-membered lactone ring macrolides against

... antibiotics and clindamycin, was recently described in pneumococci and S. pyogenes and was designated the M phenotype.10 The majority of macrolide-resistant S. pyogenes and S. pneumoniae strains collected from different countries in that study belonged to the M phenotype. The macrolide efflux pump m ...
Human mutations in glucose 6-phosphate dehydrogenase reflect
Human mutations in glucose 6-phosphate dehydrogenase reflect

... sequence from Rhodobacter capsulatus was retrieved from the archive of University of Chicago. The full genomes of Archaeoglobus fulgidus, Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Mycoplasma genitalium, Mycoplasma pneumoniae, and Rickettsia prowazekii are listed in GENBANK and ...
Two supernumerary marker chromosomes
Two supernumerary marker chromosomes

... Interestingly, in one case reported in the literature two similar familial marker chromosomes lead to very different clinical abnormalities (see Table 2, case 6). These phenotypic differences in a mother and child can only be explained by the higher frequency of one mosaic cell line with an addition ...
Inference of homologous recombination in bacteria using whole
Inference of homologous recombination in bacteria using whole

... disperse, diversify and adapt because DNA contains information of how organisms are related. In bacteria and archaea, genomic DNA is replicated as part of reproduction by binary fission [1]. Changes in genomic DNA can accumulate because replication is unfaithful or due to DNA damage, but might also ...
(Chapter 13): Translation of mRNA
(Chapter 13): Translation of mRNA

... The genetic information is coded within mRNA in groups of three nucleotides known as codons Copyright ©The McGraw-Hill Companies, Inc. Permission required for reproduction or display ...
Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a
Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a

... and speech was slurred. Fasciculations were seen in the tongue and in the proximal arm muscles. Reflexes of the masseter muscles and deep tendon reflexes of arms and legs were hyperactive, and Babinski sign was present. Head, arm, and leg muscles were weak. Sensory abnormalities were not found. Need ...
Biochemical and genetic analysis of leucine-, isoleucine
Biochemical and genetic analysis of leucine-, isoleucine

... studies of Beadle and Taturn (1941). In their studies with Drosophila, they succeeded in relating eye-color changes to mutationally produced blocks in the biosynthesis of eye pig­ ments, Though their experimental system was limited, from the results of their studies they hypothesized that genes cont ...
Landick R, Yanofsky C. 1987. Transcription
Landick R, Yanofsky C. 1987. Transcription

... the leader region and leader transcript, respectively. At this stage there are two options (176). If there is a deficiency of charged tRNA Trp, the translating ri bosome would stall at one of the Trp codons in the peptide coding region. If this occurred, then RNA segment 1 would be masked by the sta ...
PPT
PPT

... Linkage analysis with sparse markers mapped golden to markers on chromosome 18, but highresolution position of markers unknown. Genome sequence not completed… Hybrid cell lines not available… ...
Genetic variation at RYR1, IGF2, FUT1, MUC13, and KPL2
Genetic variation at RYR1, IGF2, FUT1, MUC13, and KPL2

... c.1843C>T mutation in 1991 (Fujii et al., 1991) many breeding companies have used the DNA diagnostic test to eliminate homozygous stress positive (TT) individuals and heterozygous carriers (TC). Therefore, the high frequency of the C allele can be explained by selection. It is noteworthy that a numb ...
Rethinking heredity, again
Rethinking heredity, again

... A fundamental assumption of classical Mendelian genetics and the evolutionary Modern Synthesis is that heredity is ‘hard’ – that is, mediated by the transmission of gene alleles that are impervious to environmental influence. By the standard historical narrative, the exclusive validity of the Mendel ...
APPROACHES  TO CARBOHYDRATE-BASED  CHEMICAL LIBRARIES:  THE
APPROACHES TO CARBOHYDRATE-BASED CHEMICAL LIBRARIES: THE

... One such approach is structure-based rational drug design.* Conceptually, rational drug design is very simple. If one can define the three-dimensional structure of a target molecule of known biological importance, then it should be possible to "design" compounds which can interact with the target in ...
Green Fluorescent Protein
Green Fluorescent Protein

... • Re-engineered GFP with preferred human codon usage • 20 fold enhancement consistent with 20 fold increase of GFP protein levels • GFP mutants can fluoresce different colors and be used simultaneously to monitor independent events in cells • Some GFP mutants exhibit more rapid formation of fluoroph ...
Rethinking heredity, again
Rethinking heredity, again

... A fundamental assumption of classical Mendelian genetics and the evolutionary Modern Synthesis is that heredity is ‘hard’ – that is, mediated by the transmission of gene alleles that are impervious to environmental influence. By the standard historical narrative, the exclusive validity of the Mendel ...
Slide 1
Slide 1

... The major energy sources for ATP resynthesis are fats and carbohydrates. However, phosphocreatine (PCr) is another high-energy phosphate that can be hydrolyzed to provide the energy to form ATP from ADP+P (it is often called an “energy reservoir”). ...
lilliputian - Development - The Company of Biologists
lilliputian - Development - The Company of Biologists

... fragments flanking the P element were isolated by plasmid rescue and used as probes to screen various cDNA libraries to isolate a large number of alternatively spliced cDNA clones, including one species that apparently encoded a full-length cDNA (Fig. 1D). Comparison of cDNA sequence to genomic sequ ...
Genetic Codes with No Dedicated Stop Codon: Context
Genetic Codes with No Dedicated Stop Codon: Context

... Other than the diversity of genetic codes in ciliates, the greatest number of variant genetic codes are found in mitochondria (Knight et al., 2001), whose diversification may have been facilitated by their small genomes and strong mutational biases, which increase the likelihood of loss and reassign ...
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Artificial gene synthesis

Artificial gene synthesis is a method in synthetic biology that is used to create artificial genes in the laboratory. Currently based on solid-phase DNA synthesis, it differs from molecular cloning and polymerase chain reaction (PCR) in that the user does not have to begin with preexisting DNA sequences. Therefore, it is possible to make a completely synthetic double-stranded DNA molecule with no apparent limits on either nucleotide sequence or size. The method has been used to generate functional bacterial or yeast chromosomes containing approximately one million base pairs. Recent research also suggests the possibility of creating novel nucleobase pairs in addition to the two base pairs in nature, which could greatly expand the possibility of expanding the genetic code.Synthesis of the first complete gene, a yeast tRNA, was demonstrated by Har Gobind Khorana and coworkers in 1972. Synthesis of the first peptide- and protein-coding genes was performed in the laboratories of Herbert Boyer and Alexander Markham, respectively.Commercial gene synthesis services are now available from numerous companies worldwide, some of which have built their business model around this task. Current gene synthesis approaches are most often based on a combination of organic chemistry and molecular biological techniques and entire genes may be synthesized ""de novo"", without the need for precursor template DNA. Gene synthesis has become an important tool in many fields of recombinant DNA technology including heterologous gene expression, vaccine development, gene therapy and molecular engineering. The synthesis of nucleic acid sequences is often more economical than classical cloning and mutagenesis procedures.
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