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Genetic engineering approaches to study of the opines of natural GMOs
- Authors: Sokornova S.V.1, Alekseeva A.N.1,2, Shaposhnikov A.D.1, Matveeva T.V.1
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Affiliations:
- Saint Petersburg State University
- Saint Petersburg State University of Industrial Technologies and Design
- Issue: Vol 20 (2022): Supplement
- Pages: 33-34
- Section: Genetically modified organism. The Нistory, Achivements, Social and Environmental Riscs
- Submitted: 05.11.2022
- Accepted: 11.11.2022
- Published: 08.12.2022
- URL: https://journals.eco-vector.com/ecolgenet/article/view/112380
- DOI: https://doi.org/10.17816/ecogen112380
- ID: 112380
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Abstract
A few dozen naturally transgenic plants have been described to date [1]. Many of them contain DNA-sequences homologous to opine biosynthesis genes. Chemically, opines fall into two major structural classes: secondary amine derivatives and sugar-phosphodiesters [2]. The concentration of these molecules in the crude plant extract of nGMOs could be less than 1 pmol, which makes it difficult to study them. However, structure clarification of plant opines reveal their function in plants. The aim of our work is the development of protocol for large scale production, purification and definition of the chemical structure of plant opines.
The approach includes amplification of full-length opine synthase gene by PCR and cloning it using pENTR™/D-TOPO™ Cloning Kit (Thermo Fisher) according to its manual; subcloning in pDest527 using LR Clonase™ II Plus enzyme (Thermo Fisher) according to its manual; transformation NiCo21(DE3) chemically competent E. coli cells with obtained recombinant plasmids. After the confirmation of transgenic nature, the E. coli cells should be grown on medium with ampicillin 100 mg/l to an optical density at 600 nm 0.5–0.6. Then an equal volume of LB medium with 1 mM isopropylthio-β-galactoside (IPTG) should be added for induction opine synthesis. In case of synthesis of sugar-phosphodiesters, cultural media should also contain 0.02 M arabinose, glucose, and sucrose, respectively. Cells are cultivated during 4 hours for induction of opine synthesis. After that cells are pelleted by centrifugation for 10 minutes at 5000 rpm/min. The original strain and cells grown on the medium without IPTG are used as controls.
The cells are extracted with 80% methanol. The culture liquids are evaporated and redissolved in 80% methanol. The opines are separated by normal-phase chromatography using a CHROMABOND® Flash BT. Thin-layer chromatography is used to analyze the fractions, and to confirm the component opines-like compounds. High-resolution mass spectra are recorded on a Bruker micrOTOF 10223 mass spectrometer (electrospray ionization), eluent 80% MeOH. The 31P NMR spectra are acquired on a Bruker Avance 400 spectrometer (400, 100, and 162 MHz, respectively). The 1H spectra are analyzed in D2O, with residual solvent signals (7.26 ppm for 1H nuclei) as the internal reference. The 31P NMR is measured relative to H3PO4.
The one phosphoric acid residue in the opine structure was confirmed by NMR spectroscopy.
We applied this method to characterize agrocinopine A-like compound in Nicotiana and propose it to produce opine-like plant compounds for further biochemical analysis.
This research was funded the Ministry of Science and Higher Education of the Russian Federation in accordance with the agreement No. 075-15-2022-322.
This work was partially carried out using equipments of the Saint Petersburg State University “Chemical Analysis and Materials Research Centre”.
Full Text
A few dozen naturally transgenic plants have been described to date [1]. Many of them contain DNA-sequences homologous to opine biosynthesis genes. Chemically, opines fall into two major structural classes: secondary amine derivatives and sugar-phosphodiesters [2]. The concentration of these molecules in the crude plant extract of nGMOs could be less than 1 pmol, which makes it difficult to study them. However, structure clarification of plant opines reveal their function in plants. The aim of our work is the development of protocol for large scale production, purification and definition of the chemical structure of plant opines.
The approach includes amplification of full-length opine synthase gene by PCR and cloning it using pENTR™/D-TOPO™ Cloning Kit (Thermo Fisher) according to its manual; subcloning in pDest527 using LR Clonase™ II Plus enzyme (Thermo Fisher) according to its manual; transformation NiCo21(DE3) chemically competent E. coli cells with obtained recombinant plasmids. After the confirmation of transgenic nature, the E. coli cells should be grown on medium with ampicillin 100 mg/l to an optical density at 600 nm 0.5–0.6. Then an equal volume of LB medium with 1 mM isopropylthio-β-galactoside (IPTG) should be added for induction opine synthesis. In case of synthesis of sugar-phosphodiesters, cultural media should also contain 0.02 M arabinose, glucose, and sucrose, respectively. Cells are cultivated during 4 hours for induction of opine synthesis. After that cells are pelleted by centrifugation for 10 minutes at 5000 rpm/min. The original strain and cells grown on the medium without IPTG are used as controls.
The cells are extracted with 80% methanol. The culture liquids are evaporated and redissolved in 80% methanol. The opines are separated by normal-phase chromatography using a CHROMABOND® Flash BT. Thin-layer chromatography is used to analyze the fractions, and to confirm the component opines-like compounds. High-resolution mass spectra are recorded on a Bruker micrOTOF 10223 mass spectrometer (electrospray ionization), eluent 80% MeOH. The 31P NMR spectra are acquired on a Bruker Avance 400 spectrometer (400, 100, and 162 MHz, respectively). The 1H spectra are analyzed in D2O, with residual solvent signals (7.26 ppm for 1H nuclei) as the internal reference. The 31P NMR is measured relative to H3PO4.
The one phosphoric acid residue in the opine structure was confirmed by NMR spectroscopy.
We applied this method to characterize agrocinopine A-like compound in Nicotiana and propose it to produce opine-like plant compounds for further biochemical analysis.
This research was funded the Ministry of Science and Higher Education of the Russian Federation in accordance with the agreement No. 075-15-2022-322.
This work was partially carried out using equipments of the Saint Petersburg State University “Chemical Analysis and Materials Research Centre”.
About the authors
Sofia V. Sokornova
Saint Petersburg State University
Email: s.sokornova@spbu.ru
ORCID iD: 0000-0001-6718-4818
SPIN-code: 3223-0513
PhD, Leading Researcher, All-Russian Institute of Plant Protection
Russian Federation, Saint PetersburgAlena N. Alekseeva
Saint Petersburg State University; Saint Petersburg State University of Industrial Technologies and Design
Email: yuyi99@mail.ru
Master’s Degree
Russian Federation, Saint Petersburg; Saint PetersburgAnton D. Shaposhnikov
Saint Petersburg State University
Email: st096319@student.spbu.ru
Master’s Degree
Russian Federation, Saint PetersburgTatiana V. Matveeva
Saint Petersburg State University
Author for correspondence.
Email: radishlet@gmail.com
SPIN-code: 3877-6598
Doctor of Science, Professor, Department of Genetics and Biotechnology
Russian Federation, Saint PetersburgReferences
- Matveeva TV. New naturally transgenic plants: 2020 update. Biol Commun. 2021;66(1): 36–46. doi: 10.21638/spbu03.2021.105
- Мatveeva TV, Otten L. Opine biosynthesis in naturally transgenic plants: Genes and products. Phytochemistry. 2021;189:112813. doi: 10.1016/j.phytochem.2021.112813
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