Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection

An efficient transformation protocol based on kanamycin selection was developed for Agrobacterium-mediated transformation of maritime pine embryonal masses. The binary vector pBINUbiGUSint, which contained neomycin phosphotransferase II (nptII) as a selectable marker gene and β-glucuronidase (uidA)...

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Main Authors: José M. Alvarez, Ricardo J. Ordás
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1155/2013/681792
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spelling doaj-94b1148321ba40a38ca87a67ca21ba372020-11-25T02:40:29ZengHindawi LimitedThe Scientific World Journal1537-744X2013-01-01201310.1155/2013/681792681792Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin SelectionJosé M. Alvarez0Ricardo J. Ordás1Laboratorio de Biotecnología Agroforestal, Escuela Politécnica de Mieres, Universidad de Oviedo, Calle Gonzalo Gutiérrez Quirós, 33600 Mieres, SpainLaboratorio de Biotecnología Agroforestal, Escuela Politécnica de Mieres, Universidad de Oviedo, Calle Gonzalo Gutiérrez Quirós, 33600 Mieres, SpainAn efficient transformation protocol based on kanamycin selection was developed for Agrobacterium-mediated transformation of maritime pine embryonal masses. The binary vector pBINUbiGUSint, which contained neomycin phosphotransferase II (nptII) as a selectable marker gene and β-glucuronidase (uidA) as a reporter gene, was used for transformation studies. Different factors, such as embryogenic line, bacterial strain, bacterial concentration, and coculture duration, were examined and optimized. For selection of transformants, 15 mgL−1 kanamycin was used. The highest transformation efficiency (11.4 events per gram of fresh mass) was achieved when a vigorously growing embryonal mass (embryogenic line L01) was cocultivated with Agrobacterium strain AGL1 at the optical density (OD600 nm) of 0.3 for 72 h. Evidence of the stable transgene integration was obtained by polymerase chain reaction for the nptII and uidA genes and expression of the uidA gene. Maturation capacity of the transgenic lines was negatively affected by the transformation process. Induction of axillary shoots by preculturing the embryos with benzyladenine allowed overcoming the low maturation rates of some transformed lines. The transgenic embryos were germinated and the axillar shoots were rooted. Transgenic plants were transferred to potting substrate showing normal growth.http://dx.doi.org/10.1155/2013/681792
collection DOAJ
language English
format Article
sources DOAJ
author José M. Alvarez
Ricardo J. Ordás
spellingShingle José M. Alvarez
Ricardo J. Ordás
Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
The Scientific World Journal
author_facet José M. Alvarez
Ricardo J. Ordás
author_sort José M. Alvarez
title Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
title_short Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
title_full Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
title_fullStr Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
title_full_unstemmed Stable Agrobacterium-Mediated Transformation of Maritime Pine Based on Kanamycin Selection
title_sort stable agrobacterium-mediated transformation of maritime pine based on kanamycin selection
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2013-01-01
description An efficient transformation protocol based on kanamycin selection was developed for Agrobacterium-mediated transformation of maritime pine embryonal masses. The binary vector pBINUbiGUSint, which contained neomycin phosphotransferase II (nptII) as a selectable marker gene and β-glucuronidase (uidA) as a reporter gene, was used for transformation studies. Different factors, such as embryogenic line, bacterial strain, bacterial concentration, and coculture duration, were examined and optimized. For selection of transformants, 15 mgL−1 kanamycin was used. The highest transformation efficiency (11.4 events per gram of fresh mass) was achieved when a vigorously growing embryonal mass (embryogenic line L01) was cocultivated with Agrobacterium strain AGL1 at the optical density (OD600 nm) of 0.3 for 72 h. Evidence of the stable transgene integration was obtained by polymerase chain reaction for the nptII and uidA genes and expression of the uidA gene. Maturation capacity of the transgenic lines was negatively affected by the transformation process. Induction of axillary shoots by preculturing the embryos with benzyladenine allowed overcoming the low maturation rates of some transformed lines. The transgenic embryos were germinated and the axillar shoots were rooted. Transgenic plants were transferred to potting substrate showing normal growth.
url http://dx.doi.org/10.1155/2013/681792
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