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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Main Authors: Mostafa M. EL-Sheekh, Adel W. Almutairi, Hussein E. Touliabah
Format: Article
Language:English
Published: Taylor & Francis Group 2019-12-01
Series:Journal of Taibah University for Science
Subjects:
Online Access:http://dx.doi.org/10.1080/16583655.2019.1603574
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spelling 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
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