Herbicide-tolerant sugarcane (Saccharum officinarum L.) plants: an unconventional method of weed removal

Unnecessary weed growth in sugarcane fields forces plants to compete for nutrients and sunlight for survival, which most often leads to significant yield losses. As chemical herbicides cannot differentiate between crop plants and weeds, the development of herbicide-tolerant crops is anticipated. Four sugarcane varieties, CPF-234, CPF-213, HSF-240, and CPF-246, were used to develop glyphosate herbicide tolerance. A glyphosate-tolerant gene of 1368 bp cloned directionally under the 35S promoter with the \Beta-glucuronidase (GUS) reporter gene was used as the transgene. Through the biolistic transformation of sugarcane, calli of all cultivars were transformed with glyphosate-tolerant gene constructs. Efficient regeneration conditions were optimized on 1.5-2.5 mg/L kinetin, 1.5-2.5 mg/L 6-benzylaminopurine (BAP), and 1 mg/L gibberellic acid (GA3). The transformants exhibited the best shoot regeneration on a medium containing 2 mg/L kinetin, 2 mg/L BAP, 2 mg/L GA3, and 1 mg/L indole-3-acetic acid. Based on initial screenings through GUS assay, the transformation efficiency was 22%, 32%, 17%, and 13% for cultivars 246, 234, 213, and 240, respectively. In transformed sugarcane plants, the transgene of 1368 bp was amplified. ELISA with gene-specific coated monoclonal IgG confirmed the transgene protein expression. It was revealed that all acclimatized transgenic sugarcane plants survived the glyphosate spray application of 900 mL/0.404 ha, except for the control nontransformed plants. However, at spray application of 1100 mL/0.404 ha, transgenic plants having the transgene protein OD of 0.2 to 1.0 did not survive, while those that had a transgene protein OD range of between 1.0 and 2.0 did. In addition, weeds growing alongside transgenic sugarcane plants turned brown and subsequently died at glyphosate spray applications of both 900 and 1100 mL/0.404 ha.

Herbicide-tolerant sugarcane (Saccharum officinarum L.) plants: an unconventional method of weed removal

Unnecessary weed growth in sugarcane fields forces plants to compete for nutrients and sunlight for survival, which most often leads to significant yield losses. As chemical herbicides cannot differentiate between crop plants and weeds, the development of herbicide-tolerant crops is anticipated. Four sugarcane varieties, CPF-234, CPF-213, HSF-240, and CPF-246, were used to develop glyphosate herbicide tolerance. A glyphosate-tolerant gene of 1368 bp cloned directionally under the 35S promoter with the \Beta-glucuronidase (GUS) reporter gene was used as the transgene. Through the biolistic transformation of sugarcane, calli of all cultivars were transformed with glyphosate-tolerant gene constructs. Efficient regeneration conditions were optimized on 1.5-2.5 mg/L kinetin, 1.5-2.5 mg/L 6-benzylaminopurine (BAP), and 1 mg/L gibberellic acid (GA3). The transformants exhibited the best shoot regeneration on a medium containing 2 mg/L kinetin, 2 mg/L BAP, 2 mg/L GA3, and 1 mg/L indole-3-acetic acid. Based on initial screenings through GUS assay, the transformation efficiency was 22%, 32%, 17%, and 13% for cultivars 246, 234, 213, and 240, respectively. In transformed sugarcane plants, the transgene of 1368 bp was amplified. ELISA with gene-specific coated monoclonal IgG confirmed the transgene protein expression. It was revealed that all acclimatized transgenic sugarcane plants survived the glyphosate spray application of 900 mL/0.404 ha, except for the control nontransformed plants. However, at spray application of 1100 mL/0.404 ha, transgenic plants having the transgene protein OD of 0.2 to 1.0 did not survive, while those that had a transgene protein OD range of between 1.0 and 2.0 did. In addition, weeds growing alongside transgenic sugarcane plants turned brown and subsequently died at glyphosate spray applications of both 900 and 1100 mL/0.404 ha.

___

  • Aasim M, Khawar KM, Özcan S (2013). Production of herbicide- resistant cowpea (Vigna unguiculata L.) transformed with the bar gene. Turk J Biol 37: 472–478.
  • Ahmad S, Saleem S, Zubair M, Khalil IA, Sohail K, Rehman Z (2012). Farmers’ practices and yield response of sugarcane in Jhang and Sargodha districts, Pakistan. Sarhad J Agric 28: 201.
  • Barampuram S, Zhang ZJ (2011). Recent advances in plant transformation. Plant chromosome engineering. Methods Mol Biol 701: 1–35.
  • Basnayake SW, Moyle R, Birch RG (2011). Embryogenic callus proliferation and regeneration conditions for genetic transformation of diverse sugarcane cultivars. Plant Cell Rep 30: 439–348.
  • Bisht NC, Burma PK, Pental D (2004). Development of 2,4-D-resistant transgenics in Indian oilseed mustard (Brassica juncea). Curr Sci 87: 367–370.
  • Busse MD, Ratcliffe AW, Shestak CJ, Powers RF (2001). Glyphosate toxicity and the effects of long-term vegetation control on soil microbial community. Soil Biol Biochem 33: 1777–1789.
  • Castle LA, Siehl DL, Gorton R, Patten PA, Chen YH, Bertain S, Cho HJ, Duck N, Wong J, Liu D et al (2004). Discovery and directed evolution of a glyphosate tolerance gene. Science 304: 1151– 1154.
  • Chengalrayan K, Abouzid A, Gallo-Meagher M (2005). In vitro regeneration of plants from sugarcane seed-derived callus. In Vitro Cell Dev 41: 477–482.
  • Chengalrayan K, Gallo-Meagher M (2001). Effect of various growth regulators on shoot regeneration of sugarcane. In Vitro Cell Dev 37: 434–439.
  • Feng PCC, Baley GJ, Clinton WP, Bunkers GJ, Alibhai MF, Paulitz TC,  Kidwell KK (2005). Glyphosate inhibits rust diseases in glyphosate-resistant wheat and soybean. P Natl Acad Sci USA 102: 17290–17295.
  • Fitch MMM, Lehrer AT, Komor E, Moore PH (2001). Elimination of Sugarcane yellow leaf virus from infected sugarcane plants by meristem tip culture visualized by tissue blot immunoassay. Plant Pathol 50: 676–680.
  • Franklin G, Arvinth S, Sheeba CJ, Kanchana M, Subramonian N (2006). Auxin pretreatment promotes regeneration of sugarcane (Saccharum spp. hybrids) midrib segment explants. Plant Growth Regul 50: 111–119.
  • Ge X, Davignon DA, Ackerman JHJ, Sammons RD (2010). Rapid vacuolar sequestration: the horseweed glyphosate resistance mechanism. Pest Manag Sci 66: 345–348.
  • Giesy JP, Dobson S, Solomon KR (2000). Ecotoxicological risk assessment for Roundup® herbicide. Rev Environ Contam Toxicol 167: 35–120.
  • Herman P, Behrens LMS, Chakraborty BM, Barycki CJ, Weeks DP (2005). A three-component dicamba O-demethylase from Pseudomonas maltophilia, Strain DI6: gene isolation, characterization, and heterozygous expression. J Biol Chem 280: 24759–24767.
  • Hiei Y, Ohta S, Komari T, Kumashiro T (1994). Efficient transformation of rice (Oryza sativa) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J 6: 271–282.
  • Jefferson RA (1987). Assaying chimeric genes in plants: the genes fusion system. Plant Mol Biol Rep 5: 387–405.
  • Joshi R, Shukla A, Sairam RK (2011). In vitro screening of rice genotypes for drought tolerance using polyethylene glycol. Acta Physiol Plant 33: 2209–2217.
  • Joyce P, Kuwahata M, Turner N, Lakshmanan P (2010). Selection system and co-cultivation medium are important determinants of Agrobacterium-mediated transformation of sugarcane. Plant Cell Rep 29: 173–183.
  • Julian KC, Chikwamba MR, Sparrow P, Fischer R, Mahoney RR, Richard M, Twyman RM (2005). Plant-derived pharmaceuticals - the road forward. Trends Plant Sci 10: 580–585.
  • Leibbrandt NB, Snyman SJ (2003). Stability of gene expression and agronomic performance of a transgenic herbicide-resistant sugarcane line in South Africa. Crop Sci 43: 671–677.
  • Manickavasagam M, Ganapathi A, Anbazhagan VR, Sudhakar B, Selvaraj N, Vasudevan A, Kasthurirengan S (2004). Agrobacterium-mediated genetic transformation and development of herbicide-resistant sugarcane (Saccharum species hybrids) using axillary buds. Plant Cell Rep 23: 134– 143.
  • Matringe M, Sailland A, Pelissier B, Roland A, Zind O (2005). p-Hydroxyphenylpyruvate dioxygenase inhibitor-resistant plants. Pest Manag Sci 61: 269–276.
  • Mitchell BJ (2003). Control of weeds in glyphosate-tolerant sugar-beet crops (Beta vulgaris). Irish J Agri Food Sci Res 42: 265–274.
  • Murashige T, Skoog F (1962). A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plantarum 15: 473–497.
  • Nawaz M, Ullah I, Iqbal N, Iqbal MZ, Javed MA (2013). Improving in vitro leaf disk regeneration system of sugarcane (Saccharum officinarum  L.) with concurrent shoot/root induction from somatic embryos. Turk J Biol 37: 726–732.
  • Owen MDK (2008). Weed species shifts in glyphosate-resistant crops. Pest Manag Sci 64: 377–387.
  • Paganelli A, Gnazzo V, Acosta H, Lopez SL, Carrasco AE (2010). Glyphosate-based herbicides produce teratogenic effects on vertebrates by impairing retinoic acid signaling. Chem Res Toxicol 23: 1586–1595.
  • Pline WA, Viator R, Wilcut JW, Edmisten KL, Thomas J, Wells R (2002). Reproductive abnormalities in glyphosate-resistant cotton caused by lower CP4-EPSPS levels in the male reproductive tissue. Weed Science 50: 438–447. Pline-Srnic W (2006). Physiological mechanisms of glyphosate resistance. Weed Technol 20: 290–300.
  • Rainbolt CR, Dusky JA (2006). Weed Management in Sugarcane – 2007. Electronic Data Information Source (EDIS) WG004. Gainesville, FL, USA: Agronomy Department, University of Florida.
  • Ramanand KN, Subhanand N, Lal M, Singh SB (2005). Plantlet regeneration through leaf callus culture in sugarcane. Sugar Tech 8: 85–87.
  • Sambrook J, Fritsh EF, Maniatis T (1989) Molecular Cloning: A Laboratory Manual. 2nd ed. New York, NY, USA: Cold Spring Harbor Laboratory Press.
  • Snyman SJ (2004). Sugarcane Transformation. In: Curtis I, editor. Transgenic Crops of the World. Amsterdam, the Netherlands: Springer, pp. 103–114.
  • Snyman SJ, Meyer GM, Richards JM, Haricharan N, Ramgareeb S, Huckett BI (2006). Refining the application of direct embryogenesis in sugarcane: effect of the developmental phase of leaf disc explants and the timing of DNA transfer on transformation efficiency. Plant Cell Rep 25: 1016–1023.
  • Tesfamariam TS, Bott I, Cakmak V, Römheld V, Neumann RG (2009). Glyphosate in the rhizosphere – role of waiting times and different glyphosate binding forms in soils for phytotoxicity to non-target plants. Eur J Agron 31: 126–132.
  • Vencill WK, Nichols RL, Webster TM, Soteres JK, Mallory-Smith C, Burgos NR, Johnson WG, McClelland MR (2012). Herbicide resistance: toward an understanding of resistance development and the impact of herbicide-resistant crops. Weed Sci 60: 2–30.
  • Weng LX, Deng H, Xu JL, Li Q, Wang L, Jiang Z, Zhang HB, Li Q, Zhang L (2006). Regeneration of sugarcane elite breeding lines and engineering of stem borer resistance. Pest Manag Sci 62: 178–187.
  • Zambrano AY, Demey JR, Gonzalez V (2003). In vitro selection of a glyphosate-tolerant sugarcane cellular line. Plant Mol Biol Rep 21: 365–373.
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Enhanced enzymatic xylose/cellulose fractionation from alkaline liquor-pretreated corn cob by surfactant addition and separate fermentation to bioethanol

Yefu CHEN, Xinxin ZHANG, Shijie ZHANG, Weijun QIN, Changhui GUO, Xuewu GUO, Dongguang XIAO

Peripheral administration of kisspeptin antagonist does not alter basal plasma testosterone but decreases plasma adiponectin levels in adult male rhesus macaques

Tanzeel HUMA, Farhad ULLA, Farnaz HANIF, Joshua D. RIZAK, Muhammad SHAHAB

Photosynthetic characteristics of red and green leaves in growing seedlings of Jatropha curcas

Munna SINGH, Sanjay RANJAN, Krishan Kumar VERMA, Uday Vashudav PATHRE, Pramod Arvind SHIRKE

Polyploidy and apomixis in accessions of Senna rugosa (G.Don) H.S.Irwin & Barneby

Kátia RESENDE, Clara PRADO, Lisete DAVIDE, Giovana TORRES

Impact of salt stress on photosystem II efficiency and antioxidant enzyme activities of safflower (Carthamus tinctorius L.) cultivars

Şeküre Çulha ERDAL, Hüsnü ÇAKIRLAR

Melatonin is effective in reducing stress-induced organ damage in Wistar albino rats

Mukaddes EŞREFOĞLU, Ayşin AKINCI, Hülya ELBE, Elif TAŞLIDERE, Aslı ÇETİN, Burhan ATEŞ

Study of exogenous oxidative stress response in Escherichia coli, Pseudomonas spp., Bacillus spp., and Salmonella spp.

İfratun NUR, Mohammad Sakil MUNNA, Rashed NOOR

Characterization of dehydrin AhDHN from Mediterranean saltbush (Atriplex halimus)

Monther Taha SADDER, Abdullah Abdulaziz AL-DOSS

Evaluation of orange peel, an industrial waste, for the production of Aspergillus sojae polygalacturonase considering both morphology and rheology effects

Nihan GÖĞÜŞ, Bengi Hakgüder TAZE, Hande DEMİR, Canan TARI, Sevcan ÜNLÜTÜRK, Marcelo Fernandez LAHORE

Efficiency of using RAPD and ISSR markers in evaluation of genetic diversity in sugar beet

Vusala IZZATULLAYEVA, Zeynal AKPAROV, Sevda BABAYEVA, Javid OJAGHI, Mehraj ABBASOV