rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Comparative studies of diverged members of the phosphotriesterase family
  name:
    name part: Arriens, Cristina Gale.
    role:
      role term: creator
  type of resource: text
  genre: bibliography
  origin info:
    place:
      place term: xx
    date issued: 2002
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: print
    extent: vii, 24 leaves : illustrations ; 28 cm.
  abstract: Some genes direct the synthesis of specific proteins called enzymes that catalyze specific types of chemical reactions. The class of enzyme of interest in this research, the hydrolases, catalyzes the conversion of functional groups to water. The phosphotriesterase (PTE) family is a subgroup of hydrolases that breaks down organophosphate compounds (OPs). Many organophosphate compounds are potent cholinesterase inhibitors, accounting for their widespread use as insecticides and nerve agents. Enzymes have been found in bacteria and higher organisms that specifically breakdown OPs. One of these enzymes, human serum paraoxonase/arylesterase (PON1), is a calcium-dependent, HDL (High Density Lipoprotein) -associated protein that appears to have multiple roles in vivo. In one guise, PON1 hydrolyses organophosphate insecticides and nerve gases and is responsible for determining the selective toxicity of these compounds in mammals. Using the sequence available in NCBI Genebank, primers flanking the coding region of PON1 were designed and used to screen a human liver cDNA library using polymerase chain reaction (PCR). A single band corresponding to the approximate size of PON1, 1kb, was amplified and subsequently cloned. The identity of the cloned region as PON1 was verified by sequencing using PON1 specific primers, and then cloned into a plasmid named pTYB1 from the IMPACT-CN expression system. Expression was obtained using the BL21-star bacterial strain. The enzyme was found within an inclusion body, and solubilized with urea and DTT. Preliminary activity studies were unsuccessful, so further manipulation of the insoluble fraction is necessary to obtain proper folding.
  note: by Cristina Gale Arriens.
  note: Vita.
  note: "Major Subject: Life Sciences I".
  note: Fellows Thesis Texas A&M University 2002.
  note: Includes bibliographical references (leaf 23).
  subject:
    topic: Major life sciences I
  identifier: http://hdl.handle.net/1969.1/ETD-TAMU-2002-Fellows-Thesis-A762
  related item:
    location:
      url: http://hdl.handle.net/1969.1/ETD-TAMU-2002-Fellows-Thesis-A762
  record info:
    record content source: TXA
    record creation date: 030605
    record change date: 20151025071520.0
    record identifier: in00001755911