Biotechnology &Amp; Biological Frontiers 2019
DOI: 10.4324/9780429050329-38
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Introduction of Genetic Material into Plant Cells

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Cited by 6 publications
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“…This plasmid contained a precise deletion of the complete internal T-DNA region, only conserving the T-DNA borders. By a simple co-integration step, it became possible to integrate any gene of interest (GOI) between both T-DNA borders (Caplan et al, 1983;Zambryski et al, 1983;Zambryski et al, 2013). Around the same time, another strategy to facilitate the cloning of a specific GOI was introduced: the binary vector system.…”
Section: Introductionmentioning
confidence: 99%
“…This plasmid contained a precise deletion of the complete internal T-DNA region, only conserving the T-DNA borders. By a simple co-integration step, it became possible to integrate any gene of interest (GOI) between both T-DNA borders (Caplan et al, 1983;Zambryski et al, 1983;Zambryski et al, 2013). Around the same time, another strategy to facilitate the cloning of a specific GOI was introduced: the binary vector system.…”
Section: Introductionmentioning
confidence: 99%
“…The most prominent ECR-type of Rhodobacterales and rhizobia are RepABC-type plasmids, whose occurrence is restricted to Alphaproteobacteria [54]. Tumour-inducing (Ti) RepABC plasmids of Agrobacterium have been intensively studied since the 1970s, and their derivatives were later used as biotechnological workhorses for plant genetics in the pre-CRISPR-Cas9 era [55,56]. However, the model system is still of scientific interest and mutations within the partitioning protein RepB have recently been correlated with the transition from a single copy to a higher copy number plasmid [57].…”
Section: Novel Insights Into the Biology Of Repabc-type Plasmids From...mentioning
confidence: 99%
“…Para resolver este problema se han desarrollado dos estrategias de clonación que facilitan la manipulación del ADN de grandes plásmidos Ti. La primera utiliza un vector intermediario (Caplan et al, 1983;Horsch et al, 1984). En este caso, se extrae la región ADN-T del plásmido Ti y se clona en un plásmido pequeño de E. coli, pBR322, que es relativamente fácil de manipular in vitro.…”
Section: Transformación De Plantas Mediada Porunclassified