Department of Biotechnology, Knowledge Unit of Science, University of Management and Technology, Sialkot Campus, Punjab, Pakistan.
Department of Plant Breeding and Genetics, University of the Punjab, Lahore, Pakistan.
PLoS One. 2024 Nov 19;19(11):e0311797. doi: 10.1371/journal.pone.0311797. eCollection 2024.
Sugarcane has been grown all around the world to meet sugar demands for industrial sector. The current sugar recovery percentage in sugarcane cultivars is dismally low which demands scientific efforts for improvements. Multiple approaches were adopted to enhance sugar contents in commercial sugarcane plants in contrast to conventional plant breeding methods. The exploitation of biotechnological methods and exploration of isomaltulose synthetic genes presented a promising solution to increase the existing low level of sugar recovery percentage in Saccharum officinarum L. Isomaltulose synthase gene II was employed and integrated into plant expression vector driven under the leaf and stem specific promoters terminated by nopaline synthase gene in a cloning strategy shown in the present study. Three gene constructs were developed in various combinations driven under promoters Zea mays ubiquitin and Cestrum Yellow Leaf Curl virus in the single and double combined stacked system. The transformation was executed in multiple formats with single transformed events, double promoter transformation events and triple construct stacked promoters in sugarcane induced calli via the particle gene gun. The transformation of ImSyGII in sugarcane genotype HSF-240 was confirmed by molecular gene analysis while expression quantification was determined through Real Time PCR. Furthermore, HPLC was also done to harvest the increased amounts of Isomaltulose in transgenic sugarcane juice. The present work upheld the enhanced ImSyGII expression in leaves owing to the exploitation of ubiquitin, while the Cestrum Yellow Leaf Curl virus promoter enhanced gene expression in sugarcane stems. The employment of three gene constructs collectively produced elite sugar lines producing more than 78% enhancements in whole sugar recovery percentage. The mature internode proved highly efficient and receptive regarding the production of isomaltulose. Quantifications and sugar contents evaluations upheld an increased Brix ratio of transgenic sugarcane lines than control lines.
全世界都在种植甘蔗,以满足工业部门对糖的需求。目前甘蔗品种的糖回收率低得令人沮丧,这需要科学努力加以提高。与传统的植物育种方法相比,人们采用了多种方法来提高商业甘蔗植物中的糖含量。生物技术方法的开发和异麦芽酮糖合成基因的探索为提高甘蔗中现有低水平的糖回收率提供了一个有希望的解决方案。在本研究中,采用异麦芽酮糖合酶基因 II,并将其整合到植物表达载体中,该载体由终止于胭脂碱合成酶基因的叶和茎特异性启动子驱动。在克隆策略中,开发了三种不同组合的基因构建体,分别由玉米泛素和茄黄花叶卷曲病毒启动子驱动。通过粒子基因枪,将转化体转化到甘蔗诱导愈伤组织中,有单转化事件、双启动子转化事件和三重构建体堆叠启动子的多种转化形式。通过分子基因分析证实了 ImSyGII 在甘蔗基因型 HSF-240 中的转化,通过实时 PCR 确定了表达量的定量。此外,还通过 HPLC 从转基因甘蔗汁中提取了更多的异麦芽酮糖。本工作利用泛素增强了 ImSyGII 在叶片中的表达,而茄黄花叶卷曲病毒启动子增强了甘蔗茎中的基因表达。三个基因构建体的共同使用产生了具有 78%以上全糖回收率提高的优质甘蔗品系。成熟节间在生产异麦芽酮糖方面表现出高效和高接受性。定量和糖含量评估表明,转基因甘蔗品系的比甜度比对照品系高。