Peningkatan Aktivitas Enzim Metabolisme Sukrosa dan Glikolisis pada Tanaman Padi Transgenik Overekspresi Gen SoSPS1

https://doi.org/10.22146/veg.114798

Ferdi Hariyanto(1), Bambang Sugiharto(2*), Netty Ermawati(3), Wahyu Indra Duwi Fanata(4)

(1) University of Jember
(2) Universitas Jember
(3) Program Studi Produksi Benih, Politeknik Negeri Jember
(4) University of Jember
(*) Corresponding Author

Abstract


Sucrose Phosphate Synthase (SPS) is a key enzyme in the sucrose biosynthesis pathway and plays an essential role in regulating sucrose accumulation in plants. Overexpression of the SPS gene has been reported to enhance sucrose accumulation and growth in various plant species. However, its effects on the dynamics of sucrose-metabolising and glycolytic enzymes in rice remain insufficiently explored. This study aimed to analyze the activities of sucrose metabolism enzymes, including SPS, invertases (acid and neutral), sucrose synthase (SuSy), and the glycolytic enzyme hexokinase (HXK) in transgenic rice plants overexpressing the SoSPS1 gene. The experiment was conducted using a completely randomized design with five genotypes, one of which was the wild type, and four transgenic rice lines, T4, T6, T8, and T9, with four replicates. The results showed that overexpression of the SoSPS1 gene led to significant increases in plant height and biomass, as well as markedly enhanced SPS activity in all transgenic rice plants compared to the wild type. Invertase activity (A-INV and N-INV) did not differ significantly among genotypes. In contrast, SuSy activity increased dramatically in transgenic lines T6, T8, and T9, suggesting that sucrose degradation in response to the genetic modification is primarily regulated through SuSy. The increase in SuSy activity was accompanied by the rise in HXK activity in the same lines (T6, T8, and T9). These results indicate that HXK subsequently phosphorylate hexose sugars, which may act as substrates for cellulose synthesis and activate the transcription factors that lead to higher biomass production. Overall, this study demonstrates that overexpression of SoSPS1 influences carbon flux and sugar metabolism, providing deeper insights into the relationship among sucrose biosynthesis, sugar sensing, and biomass enhancement in transgenic rice.


Keywords


growth; Invertase; sucrose-phosphate synthase; Sucrose Synthase; hexokinase; transgenic rice

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References

Adiredjo, A. L. 2025. Preliminary Yield Assessment of The Rice (Oryza Sativa L.) F7 Promising Lines at a Low Altitude. SABRAO Journal of Breeding and Genetics, 57(5). https://doi.org/10.54910/sabrao2025.57.5.14

Amin, M. W., Aryan, S., Habibi, N., Kakar, K., & Zahid, T. 2022. Elucidation of photosynthesis and yield performance of rice (Oryza sativa L.) under drought stress conditions. Plant Physiology Reports, 27(1): 143–151. https://doi.org/10.1007/s40502-021-00613-0

Amor, Y., Haigler, C. H., Johnson, S., Wainscott, M., & Delmer, D. P. 1995. A membrane-associated form of sucrose synthase and its potential role in synthesis of cellulose and callose in plants. Proceedings of the National Academy of Sciences of the United States of America, 92(20): 9353–9357. https://doi.org/10.1073/pnas.92.20.9353

Anur, R. M., Mufithah, N., Sawitri, W. D., Sakakibara, H., & Sugiharto, B. 2020. Overexpression of Sucrose Phosphate Synthase Enhanced Sucrose Content and Biomass Production in Transgenic Sugarcane. Plants (Basel, Switzerland), 9(2): 200. https://doi.org/10.3390/plants9020200

Bahaji, A., Li, J., Sánchez-López, Á. M., Baroja-Fernández, E., Muñoz, F. J., Ovecka, M., Almagro, G., Montero, M., Ezquer, I., Etxeberria, E., & Pozueta-Romero, J. 2014. Starch biosynthesis, its regulation and biotechnological approaches to improve crop yields. Biotechnology Advances, 32(1): 87–106. https://doi.org/10.1016/j.biotechadv.2013.06.006

Baroja-Fernández, E., Muñoz, F. J., Montero, M., Etxeberria, E., Sesma, M. T., Ovecka, M., Bahaji, A., Ezquer, I., Li, J., Prat, S., & Pozueta-Romero, J. 2009. Enhancing Sucrose Synthase Activity in Transgenic Potato (Solanum tuberosum L.) Tubers Results in Increased Levels of Starch, ADPglucose and UDPglucose and Total Yield. Plant and Cell Physiology, 50(9): 1651–1662. https://doi.org/10.1093/pcp/pcp108

Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1): 248–254. https://doi.org/10.1016/0003-2697(76)90527-3

Chibbar, R. N., Jaiswal, S., Gangola, M., & Båga, M. 2016. Carbohydrate Metabolism. In Encyclopedia of Food Grains. 161–173. Elsevier. https://doi.org/10.1016/B978-0-12-394437-5.00089-9

Cho, Y.-H., Yoo, S.-D., & Sheen, J. 2006. Regulatory Functions of Nuclear Hexokinase1 Complex in Glucose Signaling. Cell, 127(3): 579–589. https://doi.org/10.1016/j.cell.2006.09.028

Chua, T. K., Bujnicki, J. M., Tan, T.-C., Huynh, F., Patel, B. K., & Sivaraman, J. 2008. The Structure of Sucrose Phosphate Synthase from Halothermothrix orenii Reveals Its Mechanism of Action and Binding Mode. The Plant Cell, 20(4): 1059–1072. https://doi.org/10.1105/tpc.107.051193

Ciereszko, I. 2018. Regulatory roles of sugars in plant growth and development. Acta Societatis Botanicorum Poloniae, 87(2): Article 2. https://doi.org/10.5586/asbp.3583

Coleman, H. D., Yan, J., & Mansfield, S. D. 2009. Sucrose synthase affects carbon partitioning to increase cellulose production and altered cell wall ultrastructure. Proceedings of the National Academy of Sciences of the United States of America, 106(31): 13118–13123. https://doi.org/10.1073/pnas.0900188106

Fageria, N., Baligar, V., & Jones, C. A. 2010. Growth and mineral nutrition of field crops, third edition. In Growth and Mineral Nutrition of Field Crops, Third Edition. 550. https://doi.org/10.1201/b10160

Falter, C., & Voigt, C. A. 2016. Improving biomass production and saccharification in Brachypodium distachyon through overexpression of a sucrose-phosphate synthase from sugarcane. Journal of Plant Biochemistry and Biotechnology, 25(3): 311–318. https://doi.org/10.1007/s13562-015-0343-5

Fujii, S., Hayashi, T., & Mizuno, K. 2010. Sucrose synthase is an integral component of the cellulose synthesis machinery. Plant & Cell Physiology, 51(2): 294–301. https://doi.org/10.1093/pcp/pcp190

Granot, D., Kelly, G., Stein, O., & David-Schwartz, R. 2014. Substantial roles of hexokinase and fructokinase in the effects of sugars on plant physiology and development. Journal of Experimental Botany, 65(3): 809–819. https://doi.org/10.1093/jxb/ert400

Haigler, C. H., Singh, B., Zhang, D., Hwang, S., Wu, C., Cai, W. X., Hozain, M., Kang, W., Kiedaisch, B., Strauss, R. E., Hequet, E. F., Wyatt, B. G., Jividen, G. M., & Holaday, A. S. 2007. Transgenic cotton over-producing spinach sucrose phosphate synthase showed enhanced leaf sucrose synthesis and improved fiber quality under controlled environmental conditions. Plant Molecular Biology, 63(6): 815–832. https://doi.org/10.1007/s11103-006-9127-6

Huang, Z., Liu, L., Jian, L., Xu, W., Wang, J., Li, Y., & Jiang, C.-Z. 2022. Heterologous Expression of MfWRKY7 of Resurrection Plant Myrothamnus flabellifolia Enhances Salt and Drought Tolerance in Arabidopsis. International Journal of Molecular Sciences, 23(14): 7890. https://doi.org/10.3390/ijms23147890

Huber, S. C., & Huber, J. L. 1996. ROLE AND REGULATION OF SUCROSE-PHOSPHATE SYNTHASE IN HIGHER PLANTS. Annual Review of Plant Physiology and Plant Molecular Biology, 47(1), 431–444. https://doi.org/10.1146/annurev.arplant.47.1.431

Ishimaru, K., Hirotsu, N., Kashiwagi, T., Madoka, Y., Nagasuga, K., Ono, K., & Ohsugi, R. 2008. Overexpression of a Maize SPS Gene Improves Yield Characters of Potato under Field Conditions. Plant Production Science, 11(1): 104–107. https://doi.org/10.1626/pps.11.104

Koch, K. 2004. Sucrose metabolism: Regulatory mechanisms and pivotal roles in sugar sensing and plant development. Current Opinion in Plant Biology, 7(3): 235–246. https://doi.org/10.1016/j.pbi.2004.03.014

Lawson, T., & Flexas, J. 2020. Fuelling life: Recent advances in photosynthesis research. The Plant Journal, 101(4): 753–755. https://doi.org/10.1111/tpj.14698

Leister, D. 2023. Enhancing the light reactions of photosynthesis: Strategies, controversies, and perspectives. Molecular Plant, “Celebrating 15 Years of Publication” Special Issue, 16(1): 4–22. https://doi.org/10.1016/j.molp.2022.08.005

Li, G., & Zhao, Y. 2024. The critical roles of three sugar-related proteins (HXK, SnRK1, TOR) in regulating plant growth and stress responses. Horticulture Research, 11(6): uhae099. https://doi.org/10.1093/hr/uhae099

Li, J., Hu, Y., Hu, J., Xie, Q., Chen, X., & Qi, X. (2024). Sucrose synthase: An enzyme with multiple roles in plant physiology. Journal of Plant Physiology, 303: 154352. https://doi.org/10.1016/j.jplph.2024.154352

Lincoln, M. 2024. Understanding the role of glucose-sensor HEXOKINASE in seedling establishment in Arabidopsis thaliana. https://doi.org/10.7488/era/4802

Liu, J., Cheng, Y., Ruan, M., Ye, Q., Wang, R., Yao, Z., Zhou, G., Li, Z., Liu, C., & Wan, H. (2025). Roles and Regulations of Acid Invertases in Plants: Current Knowledge and Future Perspectives. Plants, 14(3): 320. https://doi.org/10.3390/plants14030320

Lunn, J. E. 2008. Sucrose Metabolism. In Encyclopedia of Life Sciences. John Wiley & Sons, Ltd. https://doi.org/10.1002/9780470015902.a0021259

Lunn, J. E., & MacRae, E. 2003. New complexities in the synthesis of sucrose. Current Opinion in Plant Biology, 6(3): 208–214. https://doi.org/10.1016/s1369-5266(03)00033-5

Maloney, V. J., Park, J.-Y., Unda, F., & Mansfield, S. D. 2015a. Sucrose phosphate synthase and sucrose phosphate phosphatase interact in planta and promote plant growth and biomass accumulation. Journal of Experimental Botany, 66(14): 4383–4394. https://doi.org/10.1093/jxb/erv101

Maloney, V. J., Park, J.-Y., Unda, F., & Mansfield, S. D. 2015b. Sucrose phosphate synthase and sucrose phosphate phosphatase interact in planta and promote plant growth and biomass accumulation. Journal of Experimental Botany, 66(14): 4383–4394.

Meng, F., Feng, N., Zheng, D., Liu, M., Zhang, R., Huang, X., Huang, A., & Chen, Z. 2023. Exogenous Hemin alleviates NaCl stress by promoting photosynthesis and carbon metabolism in rice seedlings. Scientific Reports, 13(1): 3497. https://doi.org/10.1038/s41598-023-30619-7

Miftahudin, M. 2024. Correlation And Path Analyses for Shoot Architecture, Photosynthesis, and Yield-Related Traits In Recombinant Inbred Lines of. Sabrao Journal of Breeding and Genetics, 56(4): 1609–1620. https://doi.org/10.54910/sabrao2024.56.4.26

Moore, B., Zhou, L., Rolland, F., Hall, Q., Cheng, W.-H., Liu, Y.-X., Hwang, I., Jones, T., & Sheen, J. 2003. Role of the Arabidopsis Glucose Sensor HXK1 in Nutrient, Light, and Hormonal Signaling. Science, 300(5617): 332–336. https://doi.org/10.1126/science.1080585

Mulyatama, R. A., Neliana, I. R., Sawitri, W. D., Sakakibara, H., Kim, K.-M., & Sugiharto, B. 2022. Increasing the Activity of Sugarcane Sucrose Phosphate Synthase Enhanced Growth and Grain Yields in Transgenic Indica Rice. Agronomy, 12(12): Article 12. https://doi.org/10.3390/agronomy12122949

Park, J.-Y., Canam, T., Kang, K.-Y., Ellis, D. D., & Mansfield, S. D. 2008. Over-expression of an arabidopsis family A sucrose phosphate synthase (SPS) gene alters plant growth and fibre development. Transgenic Research, 17(2): 181–192. https://doi.org/10.1007/s11248-007-9090-2

Poorter, H., Niklas, K. J., Reich, P. B., Oleksyn, J., Poot, P., & Mommer, L. 2012. Biomass allocation to leaves, stems and roots: Meta-analyses of interspecific variation and environmental control. The New Phytologist, 193(1): 30–50. https://doi.org/10.1111/j.1469-8137.2011.03952.x

Roitsch, T., & González, M.-C. 2004. Function and regulation of plant invertases: Sweet sensations. Trends in Plant Science, 9(12): 606–613. https://doi.org/10.1016/j.tplants.2004.10.009

Rolland, F., Baena-Gonzalez, E., & Sheen, J. 2006. Sugar sensing and signaling in plants: Conserved and novel mechanisms. Annual Review of Plant Biology, 57: 675–709. https://doi.org/10.1146/annurev.arplant.57.032905.105441

Ruan, Y.-L. 2012. Signaling Role of Sucrose Metabolism in Development. Molecular Plant, 5(4): 763–765. https://doi.org/10.1093/mp/sss046

Ruan, Y.-L. 2014. Sucrose Metabolism: Gateway to Diverse Carbon Use and Sugar Signaling. Annual Review of Plant Biology, 65(1): 33–67. https://doi.org/10.1146/annurev-arplant-050213-040251

Shidiqi, M. H. A., Hariyanto, F., Sugiharto, B., Ermawati, N., & Handoyo, T. 2025. Phenotypic characterization and evaluation of transgenic indica rice overexpressing SoSPS1 gene in greenhouse trials. Journal of Crop Science and Biotechnology, 28(1): 49–56. https://doi.org/10.1007/s12892-024-00262-3

Suherman, Wijayanto, S. I., Anur, R. M., Neliana, I. R., Dewanti, P., & Sugiharto, B. 2022. Field Evaluation on Growth and Productivity of the Transgenic Sugarcane Lines Overexpressing Sucrose-Phosphate Synthase. Sugar Tech, 24(6): 1689–1698. https://doi.org/10.1007/s12355-022-01121-7

Verma, A. K., Upadhyay, S. K., Verma, P. C., Solomon, S., & Singh, S. B. (2011). Functional analysis of sucrose phosphate synthase (SPS) and sucrose synthase (SS) in sugarcane (Saccharum) cultivars. Plant Biology (Stuttgart, Germany), 13(2): 325–332. https://doi.org/10.1111/j.1438-8677.2010.00379.x

Wan, H., Wu, L., Yang, Y., Zhou, G., & Ruan, Y.-L. 2018. Evolution of Sucrose Metabolism: The Dichotomy of Invertases and Beyond. Trends in Plant Science, 23(2): 163–177. https://doi.org/10.1016/j.tplants.2017.11.001

Wei, Z., Qu, Z., Zhang, L., Zhao, S., Bi, Z., Ji, X., Wang, X., & Wei, H. 2015. Overexpression of poplar xylem sucrose synthase in tobacco leads to a thickened cell wall and increased height. PloS One, 10(3): e0120669. https://doi.org/10.1371/journal.pone.0120669

Xu, S.-M., Brill, E., Llewellyn, D. J., Furbank, R. T., & Ruan, Y.-L. 2012. Overexpression of a potato sucrose synthase gene in cotton accelerates leaf expansion, reduces seed abortion, and enhances fiber production. Molecular Plant, 5(2): 430–441. https://doi.org/10.1093/mp/ssr090

Zhang, L., Sun, S., Liang, Y., Li, B., Ma, S., Wang, Z., Ma, B., & Li, M. 2021. Nitrogen Levels Regulate Sugar Metabolism and Transport in the Shoot Tips of Crabapple Plants. Frontiers in Plant Science, 12: 626149. https://doi.org/10.3389/fpls.2021.626149

Zhu, J., Qi, J., Fang, Y., Xiao, X., Li, J., Lan, J., & Tang, C. 2018. Characterization of Sugar Contents and Sucrose Metabolizing Enzymes in Developing Leaves of Hevea brasiliensis. Frontiers in Plant Science, 9. https://doi.org/10.3389/fpls.2018.00058



DOI: https://doi.org/10.22146/veg.114798

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