GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE & FUNCTION
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE & FUNCTION
批准号:
3230255
负责人:
Simon H Chang
金额:
$8.81万
依托单位国家:
美国
项目类别:
财政年份:
1983
资助国家:
美国
项目状态:
已结题
起止时间:
1983-07-01 至 1990-06-30
中文摘要
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英文摘要
Under the current support (AM31676), we have accomplished the most
important part of the project, the cloning and characterization of
two phosphofructokinase genes; one from rabbit muscle (RMPFK) and
the other from B. stearothermophilus (BsPFK). The major goal of
this proposal is the oligonucleotide directed mutagenesis of
strategically selected residues in these two proteins to elucidate
sites critical for catalytic function, allosteric regulation and
structural integrity.
(1) Expression and mutagenesis of BsPFK gene. Based on the
sequence information we have gained, this gene will be subcloned
in an inducible vector for expression, and in M13 phage for site
directed mutagenesis at pre-selected sites as described above. The
mutated proteins will be studied for enzymatic activity, allosteric
regulation and physical properties.
(2) Construction, expression and mutagenesis of RMPFK cDNA: Our
results on the DNA sequence of this gene have enhanced our
capability to construct a full-length RMPFK cDNA. We will approach
this task by reverse transcription, oligonucleotide synthesis and
an in vitro intron deletion technique. The cDNA pieces produced
will be cleaved with endonucleases known to have unique restriction
sites in the cDNA and will be linked together using DNA ligase.
The full-length cDNA so constructed will be cloned in an inducible
plasmid vector for expression in E. coli host and subcloned in M13
phage for site directed mutagenesis. The rationale for sites of
mutation is as described above. Mutated proteins will be analyzed
for enzymatic activity, allosteric control and physical biochemical
behavior.
(3) Completion of the unfinished sequence in RMPFK gene: We have
determined the DNA sequence for all 22 exons and 65% of the introns
of RMPFK gene which is 17 kbp in length. The sequences for TATA
box, cap site, polyadenylation signal site and 40% of the introns
remain to be completed. We will complete these tasks by
chromosomal walking, DNA sequencing and computer analysis of the
data.
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SMALL INSTRUMENTATION GRANT
-
批准号:2149792
-
项目类别:
-
资助金额:$2.13万
-
财政年份:1994
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE AND FUNCTION
-
批准号:3230257
-
项目类别:
-
资助金额:$14.49万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE AND FUNCTION
-
批准号:3230262
-
项目类别:
-
资助金额:$14.34万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE & FUNCTION
-
批准号:3230260
-
项目类别:
-
资助金额:$8.62万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE & FUNCTION
-
批准号:3230261
-
项目类别:
-
资助金额:$8.0万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE AND FUNCTION
-
批准号:2138667
-
项目类别:
-
资助金额:$14.86万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
GENETICS OF PHOSPHOFRUCTOKINASE STRUCTURE AND FUNCTION
-
批准号:3152322
-
项目类别:
-
资助金额:$9.11万
-
财政年份:1983
-
负责人:Simon H Chang
-
依托单位:
海外基金