Difference between revisions of "Part:BBa K4002005"
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endo-pgaA | endo-pgaA | ||
− | == | + | == Profile == |
Name: endo-pgaA | Name: endo-pgaA | ||
+ | |||
Base Pairs: 1113bp | Base Pairs: 1113bp | ||
+ | |||
Origin: Aspergillus niger SC323, genome | Origin: Aspergillus niger SC323, genome | ||
+ | |||
Properties: An enzyme degradation of pectin | Properties: An enzyme degradation of pectin | ||
+ | |||
==== Usage and Biology ==== | ==== Usage and Biology ==== | ||
Polygalacturonase is an enzyme that hydrolyzes the alpha-1,4 glycosidic bonds between galacturonic acid residues. It is also known as pectin depolymerase, PG, pectolase, pectin hydrolase, and poly-alpha-1,4-galacturonide glycanohydrolase. This part as a repair template DNA was connected with homology arm of HXK1. | Polygalacturonase is an enzyme that hydrolyzes the alpha-1,4 glycosidic bonds between galacturonic acid residues. It is also known as pectin depolymerase, PG, pectolase, pectin hydrolase, and poly-alpha-1,4-galacturonide glycanohydrolase. This part as a repair template DNA was connected with homology arm of HXK1. | ||
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== Experimental approach == | == Experimental approach == | ||
Construction of repair template | Construction of repair template | ||
− | The repair template DNA containing PgaA gene | + | The repair template DNA containing PgaA gene was generated by the overlap-PCR method. |
We determined the concentration of PgaA from recombinant S. cerevisiae strains. Samples from the culture media, total cell lysates and the soluble portion of cell lysates were collected and subjected to DNS colorimetric assay. | We determined the concentration of PgaA from recombinant S. cerevisiae strains. Samples from the culture media, total cell lysates and the soluble portion of cell lysates were collected and subjected to DNS colorimetric assay. | ||
[[File:T--Xiamen City--BBa K4002005-Figure1.png|500px|thumb|center|Table 1. Measurement of PgaA concentration and unit of activity in various samples.]] | [[File:T--Xiamen City--BBa K4002005-Figure1.png|500px|thumb|center|Table 1. Measurement of PgaA concentration and unit of activity in various samples.]] |
Latest revision as of 08:09, 21 October 2021
endo-pgaA
endo-pgaA
Profile
Name: endo-pgaA
Base Pairs: 1113bp
Origin: Aspergillus niger SC323, genome
Properties: An enzyme degradation of pectin
Usage and Biology
Polygalacturonase is an enzyme that hydrolyzes the alpha-1,4 glycosidic bonds between galacturonic acid residues. It is also known as pectin depolymerase, PG, pectolase, pectin hydrolase, and poly-alpha-1,4-galacturonide glycanohydrolase. This part as a repair template DNA was connected with homology arm of HXK1.
Experimental approach
Construction of repair template The repair template DNA containing PgaA gene was generated by the overlap-PCR method. We determined the concentration of PgaA from recombinant S. cerevisiae strains. Samples from the culture media, total cell lysates and the soluble portion of cell lysates were collected and subjected to DNS colorimetric assay.
As shown in Table. 1, the concentration of PgaA in the culture media of sample -1 and -2 were determined at about 0.034 mg/ml and 0.028 mg/ml, respectively, which were relatively higher than that of cell lysates (0.009 mg/ml and 0.007 mg/ml), suggesting that most of the PgaA proteins were secreted into the culture media. In addition, in the cell lysates of sample 1, we detected ~76% of PgaA in the soluble supernatants, implying that most of the PgaA in cells are soluble.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 431
Illegal BglII site found at 989
Illegal XhoI site found at 949 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 688
Illegal BsaI.rc site found at 190
Illegal BsaI.rc site found at 1060