Difference between revisions of "Part:BBa K5023000:Design"
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This approach holds significant potential for biotechnology and research in Chlamydomonas reinhardtii. By enhancing the heterologous expression of genes of interest, algal strains with desired characteristics can be developed, ranging from biofuel production to the synthesis of bioactive compounds. | This approach holds significant potential for biotechnology and research in Chlamydomonas reinhardtii. By enhancing the heterologous expression of genes of interest, algal strains with desired characteristics can be developed, ranging from biofuel production to the synthesis of bioactive compounds. | ||
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===References=== | ===References=== | ||
Revision as of 19:20, 8 October 2023
Bleomycin Resistance Gene
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 227
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 227
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 227
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 227
Illegal NgoMIV site found at 608
Illegal NgoMIV site found at 669 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This resistance to bleomycin gene has one rbcs intron. The insertion of an rbcs intron into the bleomycin resistance gene represents an innovative strategy for heterologous expression in Chlamydomonas reinhardtii. The rbcs gene encodes the enzyme ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO), which is essential for the carbon fixation process in photosynthesis. Introns, non-coding DNA sequences, play a crucial role in gene expression regulation and messenger RNA processing.
By inserting an rbcs intron into the bleomycin resistance gene, the aim is to enhance the gene's expression and stability in Chlamydomonas reinhardtii. This strategy may allow the alga to express the bleomycin resistance gene more efficiently, enabling its survival in the presence of the antibiotic. Additionally, the intron insertion may help prevent messenger RNA degradation and improve gene translation.
This approach holds significant potential for biotechnology and research in Chlamydomonas reinhardtii. By enhancing the heterologous expression of genes of interest, algal strains with desired characteristics can be developed, ranging from biofuel production to the synthesis of bioactive compounds.
References
GATIGNOL, A.; DURAND, H.; TIRABY, G. Bleomycin resistance conferred by a drug-binding protein. FEBS Letters, v. 230, n. 1-2, p. 171–175, 28 mar. 1988.