Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression
Plasmid pBI221aadAGUS which carried both of GUS (β-glucuronidase) and aadA (aminoglyoside transferase) genes besides of the 35S cauliflower mosaic virus promoter was constructed and used for stable nuclear transformation of Chlamydomonas reinhardtii. The vector was transformed into the alga by parti...
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Online Access: | http://dx.doi.org/10.1080/16583655.2019.1603574 |
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doaj-adec61d163c64d16aabf512200f616a32020-11-25T01:41:11ZengTaylor & Francis GroupJournal of Taibah University for Science1658-36552019-12-0113152953510.1080/16583655.2019.16035741603574Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expressionMostafa M. EL-Sheekh0Adel W. Almutairi1Hussein E. Touliabah2Tanta UniversityKing Abdulaziz UniversityKing Abdulaziz UniversityPlasmid pBI221aadAGUS which carried both of GUS (β-glucuronidase) and aadA (aminoglyoside transferase) genes besides of the 35S cauliflower mosaic virus promoter was constructed and used for stable nuclear transformation of Chlamydomonas reinhardtii. The vector was transformed into the alga by particle gun bombardment and two positive colonies were selected on spectinomycin–containing medium. The restriction analysis of the DNA of the positive colonies showed that aadA was inserted in two orientations. The presence of introduced genes in the transformed colonies was confirmed by (PCR) using primers specific to GUS and aadA genes. The expression of aadA and GUS genes was revealed in all colonies that were grown on spectinomycin in liquid culture for 3–4 generations. The usefulness of this vector, differing in the orientation of the aadA cassette, was manisfested by transforming C. reinhardtii to spectinomycin resistance in the stable expression. This constructed plasmid-based expression vector system would help to unravel the functions of various genes in the green alga.http://dx.doi.org/10.1080/16583655.2019.1603574algaetransformationplasmidgus genechlamydomonasparticle gun bombardment |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mostafa M. EL-Sheekh Adel W. Almutairi Hussein E. Touliabah |
spellingShingle |
Mostafa M. EL-Sheekh Adel W. Almutairi Hussein E. Touliabah Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression Journal of Taibah University for Science algae transformation plasmid gus gene chlamydomonas particle gun bombardment |
author_facet |
Mostafa M. EL-Sheekh Adel W. Almutairi Hussein E. Touliabah |
author_sort |
Mostafa M. EL-Sheekh |
title |
Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression |
title_short |
Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression |
title_full |
Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression |
title_fullStr |
Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression |
title_full_unstemmed |
Construction of a novel vector for the nuclear transformation of the unicellular green alga Chlamydomonas reinhardtii and its stable expression |
title_sort |
construction of a novel vector for the nuclear transformation of the unicellular green alga chlamydomonas reinhardtii and its stable expression |
publisher |
Taylor & Francis Group |
series |
Journal of Taibah University for Science |
issn |
1658-3655 |
publishDate |
2019-12-01 |
description |
Plasmid pBI221aadAGUS which carried both of GUS (β-glucuronidase) and aadA (aminoglyoside transferase) genes besides of the 35S cauliflower mosaic virus promoter was constructed and used for stable nuclear transformation of Chlamydomonas reinhardtii. The vector was transformed into the alga by particle gun bombardment and two positive colonies were selected on spectinomycin–containing medium. The restriction analysis of the DNA of the positive colonies showed that aadA was inserted in two orientations. The presence of introduced genes in the transformed colonies was confirmed by (PCR) using primers specific to GUS and aadA genes. The expression of aadA and GUS genes was revealed in all colonies that were grown on spectinomycin in liquid culture for 3–4 generations. The usefulness of this vector, differing in the orientation of the aadA cassette, was manisfested by transforming C. reinhardtii to spectinomycin resistance in the stable expression. This constructed plasmid-based expression vector system would help to unravel the functions of various genes in the green alga. |
topic |
algae transformation plasmid gus gene chlamydomonas particle gun bombardment |
url |
http://dx.doi.org/10.1080/16583655.2019.1603574 |
work_keys_str_mv |
AT mostafamelsheekh constructionofanovelvectorforthenucleartransformationoftheunicellulargreenalgachlamydomonasreinhardtiianditsstableexpression AT adelwalmutairi constructionofanovelvectorforthenucleartransformationoftheunicellulargreenalgachlamydomonasreinhardtiianditsstableexpression AT husseinetouliabah constructionofanovelvectorforthenucleartransformationoftheunicellulargreenalgachlamydomonasreinhardtiianditsstableexpression |
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1725042131539591168 |