Difference between revisions of "Part:BBa K4825003"
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<partinfo>BBa_K4825003 short</partinfo> | <partinfo>BBa_K4825003 short</partinfo> | ||
− | pinene synthase (PtPS) is a heterogenous gene from Pinus taeda that can convert GPP into pinene. PS contains | + | pinene synthase (PtPS) is a heterogenous gene from Pinus taeda that can convert GPP into pinene. PS contains N-terminal transport peptides (1-52 loci amino acid residues) in the native host and is responsible for targeting translation products to plastid, however this function is not required in yeast, and the N-terminal transport peptide might cause erring location of the enzyme, decrease in solubility or wrongful folding of the enzyme and affect the efficiency in yeasts, so the N-terminal of PtPS is truncated to form t48PtPS |
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | a heterogenous gene from Pinus taeda that can convert GPP into pinene. PS contains n-terminal transport peptides in the native host and is responsible for targeting translation products to plastid. | ||
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Latest revision as of 18:26, 11 October 2023
PS
pinene synthase (PtPS) is a heterogenous gene from Pinus taeda that can convert GPP into pinene. PS contains N-terminal transport peptides (1-52 loci amino acid residues) in the native host and is responsible for targeting translation products to plastid, however this function is not required in yeast, and the N-terminal transport peptide might cause erring location of the enzyme, decrease in solubility or wrongful folding of the enzyme and affect the efficiency in yeasts, so the N-terminal of PtPS is truncated to form t48PtPS
Usage and Biology
a heterogenous gene from Pinus taeda that can convert GPP into pinene. PS contains n-terminal transport peptides in the native host and is responsible for targeting translation products to plastid.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 223
Illegal BamHI site found at 1060 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 695