Skip to main navigation menu Skip to main content Skip to site footer

Vol. 12 No. 3 (2013)

Articles

THE USE OF TRANSGENIC PLANTS FOR THE DEVELOPMENT OF SELECTED BIOPRODUCTS – ACHIEVEMENTS OF THE POLISH SCIENTISTS

Submitted: December 9, 2020
Published: 2013-06-30

Abstract

Green biotechnology plays an important role in the modern agriculture. Recent progress in molecular biology and genetic engineering provides an opportunity of obtaining transgenic plants with improved characteristics, such as yield parameters, nutritional value, taste, biochemical composition, cold tolerance or pathogen resistance. Genetically modified plants can be used to produce a variety of recombinant proteins of biomedical or industrial significance, including enzymes, antigens, antibodies, hormones and secondary metabolites. Research on transgenic plants has been carried out in many countries. While there has been great development of green biotechnology worldwide, some significant achievements in this field can be contributed to Polish scientists. The paper presents research on genetically modified crops carried out in Polish scientific centers and its potential usage in different areas of man life.

References

Aksamit-Stachurska A., Korobczak-Sosna A., Kulma A., Szopa J., 2008. Glycosyltransferase efficiently controls phenylpropanoid pathway. BMC Biotechnol. 8(25),1–16.
Ashraf S., Singh P.K., Yadav D.K., Shahnawaz M., Mishra S., Sawant S.V., Tuli R., 2005. High level expression of surface glycoprotein of rabies virus in tobacco leaves and its immunoprotective activity in mice. J. Biotechnol. 119, 1–14.
Barański R., Klocke E., Nothnagel T., 2008. Chitinase CHIT36 from Trichoderma harzianum enhances resistance of transgenic carrot to fungal pathogens. J. Phytopathol. 156, 513–521.
Bartoszewski G., Niedziela A., Szwacka M., Niemirowicz-Szczytt K., 2003. Modification of tomato taste in transgenic plants carrying a thaumatin gene from Thaumatococcus daniellii Benth. Plant Breeding 122(4), 347–351.
Boba A., Kulma A., Kostyn K., Starzycki M., Starzycka E., Szopa J., 2011. The influence of carotenoid biosynthesis modification on the Fusarium culmorum and Fusarium oxysporum resistance in flax. Physiol. Mol. Plant P. 76, 39–47.
Czubacka A., Doroszewska T., 2010. Estimating agronomic traits of transgenic tobacco lines. Euphytica 172, 35–47.
Fedorowicz O., Bartoszewski G., Kamińska M., Stoeva P., Niemirowicz-Szczytt K., 2005. Pathogen-derived resistance to Tomato spotted wilt virus in transgenic tomato and tobacco plants. J. Amer. Soc. Hort. Sci. 130(2), 218–224.
Feuillet C., Keller B., 1998. Molecular aspects of biotic stress resistance in wheat. Proc. of the 9th Int. Wheat Genet. Symp., Saskatoon, Sakatchewan, Canada, Oral Presentations,. 1, 171–177.
Gandikota M., Kochk, A., Chen L., Ithal1 N., Fauquet C., Reddy1 A.R., 2001. Development of transgenic rice plants expressing maize anthocyanin genes and increased blast resistance. Mol. Breed. 7, 73–83.
Gasparis S., Orczyk W., Zalewski W., Nadolska-Orczyk A., 2011. The RNA-mediated silencing of one of the Pin genes in allohexaploid wheat simultaneously decreases the expression of the other, and increases grain hardness. J. Exp. Bot. 62(11), 4025–4036.
Gerszberg A., Wiktorek-Smagur A., Hnatuszko-Konka K., Łuchniak P., Kononowicz A.K., 2012. Expression of recombinant staphylokinase, a fibrin-specific plasminogen activator of bacterial origin, in potato (Solanum tuberosum L.) plants. World J. Microbiol. Biotechnol. 28, 1115–1123.
Kapusta J., Modelska A., Figlerowicz M., Pniewski T., Letellier M., Lisowa O., Yusibov V., Koprowski H., Plucienniczak A., Legocki A.B., 1999. A plant-derived edible vaccine against hepatitis B virus. FASEB J. 13, 1796–1799.
Kapusta J., Pniewski T., Wojciechowicz J., Bociąg P., Płucienniczak A., 2010. Nanogram doses of alum-adjuvanted HBs antigen induce humoral immune response in mice when orally administered. Arch. Immunol. Ther. Exp. 58, 143–151.
Karpiński S., Szechyńska-Hebda M., Wituszyńska W., Burdiak P., 2012. Light acclimation, retrograde signalling, cell death and immune defences in plants. Plant Cell Environ. DOI: 10.1111/pce.12018.
Kong Q., Richter L., Yang Y.F., Arntzen C.J., Mason H.S., Thanavala Y., 2001. Oral immunization with hepatitis B surface antigen expressed in transgenic plants. Proc. Natl. Acad. Sci. USA 98(20), 11539–11544.
Kosieradzka I., Sawosz E., Pastuszewska B., Szwacka M., Malepszy S., Bielecki W., Czumińska K., 2001. The effect of feeding diets with genetically modified cucumbers on the growth and health status of rats. J. Anim. Feed Sci. 10(2) suppl., 7–12.
Kowalczyk K., 2004. Identyfikacja supresora locus Pm8 w polskich odmianach pszenicy zwyczajnej (Triticum aestivum L.). Annales UMCS, Sec. E Agricultura 91(1), 485–491.
Kowalczyk K., Gruszecka D., 2010. Are genetically modified organisms (GMO) the future of nutritional economy of the Lublin region. In: Lublin region – ecological region of the XXI century. Wyd. Dom Organizatora: 29–53.
Kowalczyk K., Gruszecka D., Nowak M., Leśniowska-Nowak J., 2011. Resistance of Triticale Hybrids with Pm4b and Pm6 Genes to Powdery Mildew. Acta Biologica Cracoviensia, Series Botanica, 53(1), 57–62.
Kowalczyk K., Okoń S., Leśniowska-Nowak J., Nowak M., 2009. Wykorzystanie genów odporności na rdzę brunatną Lr19, Lr21, Lr35 w programach hodowlanych pszenicy zwyczajnej w Polsce. Zesz. Probl. Post. Nauk Roln. 542, 255–260.
Lorenc-Kukuła K., Amarowicz R., Oszmiański J., Doermann P., Starzycki M., Skała J., Żuk M., Kulma A., Szopa J., 2005a. Pleiotropic effect of phenolic compounds content increases in transgenic flax plant. J. Agric. Food Chem. 53, 3685–3692.
Lorenc-Kukuła K., Jafra S., Oszmiański J., Szopa J., 2005b. Ectopic expression of anthocyanin 5-O-glucosyltransferase in potato tuber causes increased resistance to bacteria. J. Agric. Food Chem. 53, 272–281.
Lorenc-Kukuła K., Żuk M., Kulma A., Czemplik M., Kostyn K., Skala J., Starzycki M., Szopa J., 2009. Engineering flax with the GT family 1 Solanum sogarandinum glycosyltransferase SsGT1 confers increased resistance to Fusarium infection. J. Agric. Food Chem. 57, 6698–6705.
Łukaszewicz M., Matysiak-Kata I., Skała J., Fecka I., Cisowski W., Szopa J., 2004. Antioxidant capacity manipulation in transgenic potato tuber by changes in phenolic com pounds content. J. Agric. Food Chem. 52, 1526–1533.
Masuda T., Kitabatake N., 2006. Developments in biotechnological production of sweet proteins. J. Biosci. Bioeng. 102(5), 375–389.
Musialak M., Wróbel-Kwiatkowska M., Kulma A., Starzycka E., Szopa J., 2008. Improving retting of fibre through genetic modification of flax to express pectinases. Transgenic Res. 17, 133–147.
Navabi A., Singh R.P., Tewari J.P., Briggs K.G., 2004. Inheritance of high levels of adult-plant resistance to stripe rust in five spring wheat genotypes. Crop Sci. 44, 1156–1162.
Niggeweg R., Michael A.J., Martin C., 2004. Engineering plants with increased levels of the antioxidant chlorogenic acid. Nat. Biotechnol. 22, 746–754.
Pham N.B., Schäfer H., Wink M., 2012. Production and secretion of recombinant thaumatin in tobacco hairy root cultures. Biotechnol. J. 7(4), 537–545.
Pniewski T., Kapusta J., Bociąg P., Kostrzak A., Fedorowicz-Strońska O., Czyż M., Gdula M., Krajewski P., Wolko B., Płucienniczak A., 2012. Plant expression, lyophilisation and storage of HBV medium and large surface antigens for a prototype oral vaccine formulation. Plant Cell. Rep. 31, 585–595.
Pniewski T., Kapusta J., Bociąg P., Wojciechowicz J., Kostrzak A., Gdula M., Fedorowicz-Strońska O., Wójcik P., Otta H., Samardakiewicz S., Wolko B., Płucienniczak A., 2011. Lowdose oral immunization with lyophilized tissue of herbicide-resistant lettuce expressing hepatitis B surface antigen for prototype plant-derived vaccine tablet formulation. J. Appl. Genetics 52, 125–136.
Rajam M.V., Chandola N., Saiprasad Goud P., Singh D., Kashyap V., Choudhary M.L., Sihachakr D., 2007. Thaumatin gene confers resistance to fungal pathogens as well as tolerance to abiotic stresses in transgenic tobacco plants. Biol. Plant. 51(1), 135–141.
Redkiewicz P., Więsyk A., Góra-Sochacka A., Sirko A., 2012. Transgenic tobacco plants as production platform for biologically active human interleukin 2 and its fusion with proteinase inhibitors. Plant Biotechnol. J. 10, 806–814.
Rendi-Wagner P., Shouval D., Genton B., Lurie Y., Rümke H., Boland G., Cerny A., Heimh M., Bachi D., Schroeder M., Kollaritsch H., 2006. Comparative immunogenicity of a PreS/S hepatitis B vaccine in non- and low responders to conventional vaccine. Vaccine 24, 2781–2789.
Rojas-Anaya E., Loza-Rubio E., Olivera-Flores M.T., Gomez-Lim M., 2009. Expression of rabies virus G protein in carrots (Daucus carota). Trans. Res. 18, 911–919.
Schestibratov K.A., Dolgov S.V., 2005. Transgenic strawberry plants expressing a thaumatin II gene demonstrate enhanced resistance to Botrytis cinerea. Sci. Hort. 106, 177–189.
Skórkowska-Telichowska K., Żuk M., Kulma A., Bugajska-Prusak A., Ratajczak K., Gąsiorowski K., Kostyn K., Szopa J., 2010. New dressing materials derived from transgenic flax products to treat long-standing venous ulcers – a pilot study. Wound Rep. Reg. 18, 168–179.
Szechyńska-Hebda M., Kruk J., Górecka M., Karpińska B., Karpiński S., 2010. Evidence for light wavelength-specific photoelectrophysiological signaling and memory of excess light episodes in Arabidopsis. The Plant Cell 22, 2201–2218.
Szopa J., Wróbel-Kwiatkowska M., Kulma A., Żuk M., Skórkowska-Telichowska K., Dymińska L., Mączka M., Hanuza J., Zebrowski J., Preisner M., 2009. Chemical composition and molecular structure of fibers from transgenic flax producing polyhydroxybutyrate, and mechanical properties and platelet aggregation of composite materials containing these fibers. Compos. Sci. Technol. 69, 2438–2446.
Szwacka M., Burza W., Zawirska-Wojtasiak R., Gośliński M., Twardowska A., Gajc-Wolska J., Kosieradzka I., Kiełkiewicz M., 2012. Genetically modified crops expressing 35S-thaumatin II transgene: sensory properties and food safety aspects. Compr. Rev. Food Sci. Food Safety 11, 174–186.
Szwacka M., Krzymowska M., Osuch A., Kowalczyk M.E., Malepszy S., 2002. Variable properties of transgenic cucumber plants containing the thaumatin II gene from Thaumatococcus daniellii. Acta Physiol. Plant. 24(2), 173–185
Tacket C.O., Mason H.S., Losonsky G., Estes M.K., Levine M.M., Arntzen C.J., 2000. Human Immune Responses to a Novel Norwalk Virus Vaccine Delivered in Transgenic Potatoes. J. Infect. Dis. 182, 302–305.
Thanavala Y., Mahoney M., Pal S., Scott A., Richter L., Natarajan N., Goodwin P., Arntzen C.J., Mason H.S., 2005. Immunogenicity in humans of an edible vaccine for hepatitis B. Proc. Natl. Acad. Sci. USA 102(9), 3378–3382.
Treutter D., 2005. Significance of flavonoids in plant resistance and enhancement of their biosynthesis. Plant Biology 7(6), 581–591.
Witty M., 1990. Preprothaumatin II is processed to biological activity in Solanum tuberosum. Biotechnol. Lett.12(2), 131–136.
Wróbel-Kwiatkowska M., Lorenc-Kukuła K., Starzycki M., Oszmiański J., Kepczyńska E., Szopa J., 2004. Expression of β-1,3-glucanase in flax causes increased resistance to fungi. Physiol. Mol. Plant P. 65, 245–256.
Wróbel-Kwiatkowska M., Skórkowska-Telichowska K., Dymińska L., Mączka M., Hanuza J., Szopa J., 2009. Biochemical, mechanical, and spectroscopic analyses of genetically engineered flax fibers producing bioplastic (poly-β-hydroxybutyrate). Biotechnol. Prog. 25(5), 1489–1498.
Wróbel-Kwiatkowska M., Starzycki M., Zebrowski J., Oszmiański J., Szopa J., 2007a. Lignin deficiency in transgenic flax resulted in plants with improved mechanical properties. J. Biotech. 128, 919–934.
Wróbel-Kwiatkowska M., Zebrowski J., Starzycki M., Oszmiański J., Szopa J., 2007b. Engineering of PHB synthesis caused improved elastic properties of flax fibres. Biotech. Prog. 23, 269–277.
Yin Z., Rorat T., Szabala B.M., Ziółkowska A., Malepszy S., 2006. Expression of a Solanum sogarandinum SK3-type dehydrin enhances cold tolerance in transgenic cucumber seedlings. Plant Sci. 170, 1164–1172.
Yusibov V., Hooper D.C., Spitsin S.V., Fleysh N., Kean R.B., Mikheeva T., Deka D., Karasev A., Cox S., Randall J., Koprowski H., 2002. Expression in plants and immunogenicity of plant virus-based experimental rabies vaccine. Vaccine 20, 3155–3164.
Yusibov V., Streatfield S.J., Kushnir N., 2011. Clinical development of plant-produced recombinant pharmaceuticals. Vaccines, antibodies and beyond. Hum. Vaccin. 7(3), 313–321.
Zalewski W., Galuszka P., Gasparis S., Orczyk W., Nadolska-Orczyk A., 2010. Silencing of the HvCKX1 gene decreases the cytokinin oxidase/dehydrogenase level in barley and leads to higher plant productivity. J. Exp. Bot. 61(6), 1839–1851.
Zanetti A.R., Damme P., Shouval D., 2008. The global impact of vaccination against hepatitis B: A historical overview. Vaccine 26, 6266–6273.
Zawirska-Wojtasiak R., Gośliński M., Szwacka M., Gajc-Wolska J., Mildner-Szkudlarz S., 2009. Aroma evaluation of transgenic, thaumatin II-producing cucumber fruits. J. Food Sci. 74(3), C204-C210.
Zhang X., Buehner N.A., Hutson A.M., Estes M.K., Mason H.S., 2006. Tomato is a highly effective vehicle for expression and oral immunization with Norwalk virus capsid protein. Plant Biotechnol. J. 4, 419–432.
Zuckerman J.N., Zuckerman A.J., Symington I., Du W., Williams A., Dickson B., Young M.D., UK Hepacare Study Group, 2001. Evaluation of a new hepatitis B triple-antigen vaccine in inadequate responders to current vaccines. Hepatology 34, 798–802.
Żuk M., Kulma A., Dymińska L., Szołtysek K., Prescha A., Hanuza J., Szopa J., 2011. Flavonoid engineering of flax potentiate its biotechnological application. BMC Biotechnol. 11(10), 1–19.

Downloads

Download data is not yet available.

Similar Articles

1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.