Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1999-3-16
pubmed:abstractText
A gene coding for salmon calcitonin precursor (sCT-Gly) was amplified from salmon genomic DNA by Polymerase Chain Reaction (PCR) and fused to the expression and secretion signals of melC1 amplified by PCR. The fusion gene was cloned into the Streptomyces vector pIJ680 and expressed under the control of aminoglycoside phosphotransferase gene (aph) promoter. Streptomyces lividans TK54 transformed with the expression plasmid (pMS680) secreted biologically active sCT-Gly into the culture medium which was confirmed by Enzyme Immunoassay (EIA) and bioassay. Production of sCT-Gly by the recombinant strain in YEME medium reached a maximum of 100 micrograms/L culture at about 96 h. The recombinant sCT-Gly had almost the same HPLC retention time as the standard sCT obtained from Sigma.
pubmed:language
chi
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0379-4172
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
287-93
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
[Secretory expression of salmon calcitonin in Streptomyces lividans].
pubmed:affiliation
Institute of Medicinal Biotechnology the Chinese Academy of Medical Sciences, Beijing.
pubmed:publicationType
Journal Article, English Abstract, Research Support, Non-U.S. Gov't