scholarly journals A simple method for in planta tomato transformation by inoculating floral buds with a sticky Agrobacterium tumefaciens suspension

Author(s):  
Chika Honda ◽  
Kaoru Ohkawa ◽  
Hiroaki Kusano ◽  
Hiroshi Teramura ◽  
Hiroaki Shimada
2017 ◽  
Vol 17 (2) ◽  
pp. 49
Author(s):  
Edy Listanto ◽  
Eny Ida Riyanti ◽  
Sustiprijatno Sustiprijatno

<p class="abstrakInggris"><span>Maize (<em>Zea mays</em> L.) productivity in Indonesia is challenged to be increased using genetic engineering. Recent advances in <em>Agrobacterium tumefaciens</em>-mediated <em>in-planta</em> transforma-tion makes it possible<strong> </strong>to<strong> </strong>transform maize with low cost, and simple method. This study aimed to confirm pIG121Hm-<em>Cs</em> plasmid in <em>A. tumefaciens</em>, and to estimate the efficiency level of<strong> </strong> <em>A<strong>. </strong>tumefaciens</em>-mediated <em>in-planta</em> transformation of Indonesian maize by<strong> </strong>using pIG121Hm-<em>Cs</em> plasmid containing <em>npt</em>II and<strong> </strong><em>hpt</em><strong> </strong>genes. A series of studies were conducted including confirmation of gene construct of pIG121Hm-<em>Cs</em> plasmid in <em>A. tumefaciens</em>, transformation of four maize lines through <em>A. tumefaciens</em>-mediated <em>in-planta</em> technique, acclimatization of transformant plants and molecular analysis of selected plants using polymerase chain reaction (PCR). The pIG121Hm-<em>Cs</em> plasmid was confirmed via PCR analysis using specific primers of <em>npt</em>II and <em>hpt</em> genes and resulted 700 bp and 500 bp for fragments of <em>npt</em>II and <em>hpt</em>, respectively. After selection, acclimatization and molecular analysis steps, the efficiency levels of transformation of four maize lines were low, ranging from 3.8% to 12.8%. The level of transformation efficiency of ST-27 line was the highest accounting for 12.8% of 45 planted embryos on selection medium based on PCR analysis using specific primer for <em>npt</em>II gene. Overall, <em>A. tumefaciens</em>-mediated <em>in planta</em> transformation on maize floral pistil in this study proved to be successful and rapid. Therefore, this enhanced transformation method will be beneficial for Indonesian maize genetic engineering.</span></p>


2009 ◽  
Vol 22 (5) ◽  
pp. 529-537 ◽  
Author(s):  
Elise Haudecoeur ◽  
Mélanie Tannières ◽  
Amélie Cirou ◽  
Aurélie Raffoux ◽  
Yves Dessaux ◽  
...  

The phytopathogen Agrobacterium tumefaciens C58 expresses two lactonases, AttM and AiiB. We showed that expression of the aiiB gene was controlled by agrocinopines A and B and required the agrocinopine-ABC transporter Acc, but was not affected by the level of quorum-sensing (QS) signal 3-oxo-octanoylhomoserine lactone (OC8-HSL). In the presence of agrocinopines, a constructed aiiB mutant accumulated OC8-HSL at a level 10-fold higher than that of the wild-type strain, and showed an exacerbated expression of a key QS-regulated function, conjugation of Ti plasmid (in vitro and in planta), as well as an increase of the number of emerging tumors on the host plant. The expression and acyl-HSL-degrading activity of AttM were evident in the presence of wounded tissues; however, in unwounded plant tumors, the QS-regulated functions were weakly affected in an attM mutant. By contrast, we observed that attM conferred a selective advantage in the course of colonization of plant tumors. Finally, polymerase chain reaction survey of genes attM and aiiB showed that they were not strictly conserved in the genus Agrobacterium. This work proved that the lactonases AttM and AiiB are regulated by different plant signals and are implicated in different functions in the course of the A. tumefaciens C58–host interaction.


2006 ◽  
Vol 102 (3) ◽  
pp. 162-170 ◽  
Author(s):  
Putu Supartana ◽  
Tsutomu Shimizu ◽  
Masahiro Nogawa ◽  
Hidenari Shioiri ◽  
Tadashi Nakajima ◽  
...  

Author(s):  
Ni Putu Ayu Erninda Oktaviani Suputri ◽  
Rindang Dwiyani ◽  
Ida Ayu Putri Darmawanti ◽  
Bambang Sugiharto

The SoSPS1 gene of sugar cane plants previously subjected to Agrobacterium tumefacienmediated cloning was to be transferred to citrus plants to increase metabolism of sucrose in plant. The T-DNA harbored the SoSPS1 gene under the control of the CaMV 35S promoter from the cauliflower mosaic virus and contained the NPTII gene (kanamycin resistance gene) as a selectable marker for transformant selection. Generally, gene transformation in plants is carried out by tissue culture. However, tissue culture has several disadvantages such as its being time-consuming, its sometimes resulting in somatic mutations and somaclonal variations, and the requirement of sterile conditions in the procedure of gene transfer. In planta transformation is a useful system for those plants that lack tissue culture and regeneration system. The main function of in planta transformation is to recover the advantages of tissue culture as an efficient, quick method, including its ability to produce a large number of transgenic plants and to accumulate a high concentration of total soluble protein in short time. There are two procedures of in planta transformation for the seeds of citrus plants, namely “prick and coat” and “seed tip-cutting and imbibition”. In the prick and coat method, seeds are pricked on their entire surfaces and smeared with a suspension of Agrobacterium tumefaciens. In the seed tip-cutting and imbibition method, on the other hand, seeds are cut at the tip and soaked in a suspension of Agrobacterium tumefaciens. The leaves derived from seeds treatment were taken as samples for DNA extraction and PCR using primers of the NPTII gene (Forward: 5’-GTCATCTCACCTTCCTCCTGCC-3’; Reverse: 5’-GTCGCTTGGTCGGTCATTTCG-3’). This research found that only the seed tip-cutting and imbibition plants amplified along the 550-bp band, while those of the prick and coat method did not. Additionally, the T-DNA was successfully integrated into the genome of the plants treated with the seed tip-cutting and imbibition method but not with the prick and coat.


2019 ◽  
Vol 138 (2) ◽  
pp. 229-237 ◽  
Author(s):  
Raghavendra Aminedi ◽  
Deepa Dhatwalia ◽  
Varsha Jain ◽  
Ramcharan Bhattacharya

2017 ◽  
Vol 214 ◽  
pp. 174-179 ◽  
Author(s):  
Yong-yan Zhang ◽  
Dong-min Zhang ◽  
Yun Zhong ◽  
Xiao-jun Chang ◽  
Min-lun Hu ◽  
...  

Author(s):  
I Putu Wahyu Sanjaya ◽  
Rindang Dwiyani ◽  
I Gede Putu Wirawan ◽  
Bambang Sugiharto

One of the modern plant breedings through genetic engineering is Agrobacterium tumefaciens-mediated transformation. Agrobacterium tumefaciens-mediated transformation can be performed in vitro or in planta. In planta transformation arises from the weaknesses of the in vitro method such as need high hygiene standard, professional tissue culture experts, and more time to prepare explants and somaclonal variation. In planta transformation is a method to transfer the gene to the plant genome without any tissue culture stages. The aims of this research were to know the possibility of the prick and soak in planta method with the target of tomato seeds and to know the most suitable inoculation time for tomato seeds transformation by prick and soak method the transformation is done by pricking the seeds and soaking them in the A. tumefaciens suspension. The treatments in this study were 1 and 2 days inoculation time to test the efficacy of prick and soak in planta transformation method. Tomato seeds were pricked with a needle on the center once, and then soaked in A. tumefaciens strain LB4404 suspension carrying pKYS-SoSPS1 plasmid with Neomycin Phosphotransferase (NPTII) and Saccharum officinarum Sucrose Phosphate synthase (SoSPS1) genes. Visualization of tomato’s DNA samples after PCR showed that 1-day inoculation sample was positively integrated with NPTII gene and negative in the 2 days inoculation treatment.


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