<?xml version="1.0" encoding="UTF-8"?>
<mods xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://www.loc.gov/mods/v3" version="3.1" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
  <titleInfo>
    <title>Heterologous expression and characterization of Penicillium citrinum nuclease P1 in Aspergillus niger and its application in the production of nucleotides</title>
  </titleInfo>
  <name type="personal">
    <namePart>Chen, X.</namePart>
  </name>
  <name type="personal">
    <namePart>Wang, B.</namePart>
  </name>
  <name type="personal">
    <namePart>Pan, L.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">xx</placeTerm>
    </place>
    <dateIssued encoding="marc">9999</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">und</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">electronic</form>
  </physicalDescription>
  <abstract>Nuclease P1 gene (nuc P1)which was cloned from Penicillium citrinum and expressed in A percent niger Bdel4 with the low-background extracellular protein percent The expression strategy of multi-copy nuc P1 in the A percent niger with the linker of 2A peptide was applied to improve the enzyme activity of nuclease P1, the highest activity up to 77 percent6 U/mL percent After Ni-chelate purification, the specific enzyme activity, the optimum temperature and pH were 32 percent4 U/mg, 65 °C and 5 percent3 respectively percent The recombination nuclease P1 was activated by addition of Mg2+, Zn2+ and Cu2+, and inhibited by addition of Ca2+, Fe2+, Mn2+, Ni2+, Co2+, Mg2+, K+ and EDTA percent Furthermore, the enzyme hydrolyses yeast RNA efficiently into 5'- nucleotides percent Through enzymolysis, the highest concentration of nucleotides achieved 15 percent12 mg/mL, and 75U nuclease P1 is suitable amount should be added to the enzymolysis system percent</abstract>
  <subject>
    <topic>NUCLEASE P1</topic>
  </subject>
  <subject>
    <topic>2A PEPTIDE</topic>
  </subject>
  <subject>
    <topic>ASPERGILLUS NIGER</topic>
  </subject>
  <subject>
    <topic>RECOMBINANT EXPRESSION</topic>
  </subject>
  <relatedItem type="series">
    <titleInfo>
      <title>Protein Expression and Purification, 156, p.36-43, 2019</title>
    </titleInfo>
  </relatedItem>
  <identifier type="uri">https://drive.google.com/file/d/1cdWXN6i5MW7SVTdg7BpPxfXHslcZx-zd/view?usp=drivesdk</identifier>
  <location>
    <url>https://drive.google.com/file/d/1cdWXN6i5MW7SVTdg7BpPxfXHslcZx-zd/view?usp=drivesdk</url>
  </location>
  <recordInfo>
    <recordContentSource authority="marcorg"/>
    <recordCreationDate encoding="marc">250602</recordCreationDate>
    <recordChangeDate encoding="iso8601">20260521091741.0</recordChangeDate>
  </recordInfo>
</mods>
