USING MANNOSE AS A POSITIVE SELECTION OF TRANSFORMED CARICA PAPAYA L. VAR ‘EKSOTIKA’

2015 ◽  
Vol 77 (31) ◽  
Author(s):  
Roslinda A. Razak ◽  
Rogayah Sekeli ◽  
Noor Azmi Shaharuddin ◽  
Janna Ong Abdullah

The main objective of this study is to develop marker-free transgenic papaya plants via positive selection using phosphomannose isomerase (pmi) gene. Phosphomannose isomerase (PMI) is an enzyme that converts mannose-6-phosphate to fructose-6-phosphate, a glycolysis intermediate that supports the growth of plant cells. To establish a marker-free positive selection system using this PMI, the effect of mannose on the growth and development of embryogenic ‘Eksotika’ papaya callus was evaluated. One-month old embryogenic calli were cultured on Murashige and Skoog (MS) medium in which 60 g/L sucrose in the original recipe was replaced with different concentrations of mannose and sucrose. Mannose was supplied as the sole carbon source or in combination with sucrose at 0, 5, 10, 15, 20, 25 or 30 g/L. Embryogenic calli cultured on medium supplemented with a ratio of 0:60 g/L mannose: sucrose was used as a control. The results after six sub-cultures showed that most of the embryogenic calli transferred on media containing only mannose turned brown. Higher concentrations of mannose resulted in higher percentage of brown calli (dead). Mannose at 30 g/L mannose was found to be effective for screening transformed embryogenic calli.  Evaluation of papaya transformation efficiency using this positive selection system was pursued using 650 one-month-old embryogenic calli Agrobacterium-transformed with pNOV2819 harboring the pmi gene. Only transformed cells are capable of utilizing mannose as a carbon source to grow. After five months on mannose selection, all 67 putative transformants obtained were PCR-positives for the pmi gene.

2019 ◽  
Vol 366 (17) ◽  
Author(s):  
Kristen R Farley ◽  
William W Metcalf

ABSTRACT A repertoire of sophisticated genetic tools has significantly enhanced studies of Methanosarcina genera, yet the lack of multiple positive selectable markers has limited the types of genetic experiments that can be performed. In this study, we report the development of an additional positive selection system for Methanosarcina that utilizes the antibiotic nourseothricin and the Streptomyces rochei streptothricin acetyltransferase (sat) gene, which may be broadly applicable to other groups of methanogenic archaea. Nourseothricin was found to inhibit growth of four different methanogen species at concentrations ≤300 μg/ml in liquid or on solid media. Selection of nourseothricin resistant transformants was possible in two genetically tractable Methanosarcina species, M. acetivorans and M. barkeri, using the sat gene as a positive selectable marker. Additionally, the sat marker was useful for constructing a gene deletion mutant strain of M. acetivorans, emphasizing its utility as a second positive selectable marker for genetic analyses of Methanosarcina genera. Interestingly, two human gut-associated methanogens Methanobrevibacter smithii and Methanomassillicoccus luminyensis were more sensitive to nourseothricin than either Methanosarcina species, suggesting the nourseothricin-sat gene pair may provide a robust positive selection system for development of genetic tools in these and other methanogens.


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2021 ◽  
Author(s):  
Thomaz Mansini Carrenho Fabrin ◽  
Luciano Seraphim Gasques ◽  
Rodrigo Junio da Graça ◽  
Sônia Maria Alves Pinto Prioli ◽  
Weferson Júnio da Graça ◽  
...  

Immunology ◽  
2015 ◽  
Vol 145 (1) ◽  
pp. 161-169 ◽  
Author(s):  
Julien Sirois ◽  
Jean-François Daudelin ◽  
Salix Boulet ◽  
Miriam Marquis ◽  
Sylvain Meloche ◽  
...  

PLoS Genetics ◽  
2005 ◽  
Vol 1 (3) ◽  
pp. e41 ◽  
Author(s):  
Fuli Yu ◽  
Pardis C Sabeti ◽  
Paul Hardenbol ◽  
Qing Fu ◽  
Ben Fry ◽  
...  

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