Department of Agronomy and Plant Breading, Agriculture Faculty, Zanjan University, Zanjan, Iran.
Department of Cell and Molecular Biology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran.
BMC Biotechnol. 2024 May 24;24(1):35. doi: 10.1186/s12896-024-00859-0.
Fusarium head blight (FHB) is a devastating fungal disease affecting different cereals, particularly wheat, and poses a serious threat to global wheat production. Chitinases and β-glucanases are two important proteins involved in lysing fungal cell walls by targeting essential macromolecular components, including chitin and β-glucan micro fibrils. In our experiment, a transgenic wheat (Triticum aestivum) was generated by introducing chitinase and glucanase genes using Biolistic technique and Recombinant pBI121 plasmid (pBI-ChiGlu (-)). This plasmid contained chitinase and glucanase genes as well as nptII gene as a selectable marker. The expression of chitinase and glucanase was individually controlled by CaMV35S promoter and Nos terminator. Immature embryo explants from five Iranian cultivars (Arta, Moghan, Sisun, Gascogen and A-Line) were excised from seeds and cultured on callus induction medium to generate embryonic calluses. Embryogenic calluses with light cream color and brittle texture were selected and bombarded using gold nanoparticles coated with the recombinant pBI-ChiGlu plasmid. Bombarded calluses initially were transferred to selective callus induction medium, and later, they were transfferd to selective regeneration medium. The selective agent was kanamycin at a concentration of 25 mg/l in both media. Among five studied cultivars, A-Line showed the highest transformation percentage (4.8%), followed by the Sisun, Gascogen and Arta in descending order. PCR and Southern blot analysis confirmed the integration of genes into the genome of wheat cultivars. Furthermore, in an in-vitro assay, the growth of Fusarium graminearum was significantly inhibited by using 200 μg of leaf protein extract from transgenic plants. According to our results, the transgenic plants (T) showed the resistance against Fusarium when were compared to the non-transgenic plants. All transgenic plants showed normal fertility and no abnormal response was observed in their growth and development.
镰刀菌穗腐病(FHB)是一种严重影响不同谷物,尤其是小麦的破坏性真菌病害,对全球小麦生产构成严重威胁。几丁质酶和β-葡聚糖酶是两种重要的蛋白质,通过靶向包括几丁质和β-葡聚糖微纤维在内的重要大分子成分,参与裂解真菌细胞壁。在我们的实验中,通过生物弹射击技术和 Recombinant pBI121 plasmid(pBI-ChiGlu(-))引入几丁质酶和葡聚糖酶基因,生成了转基因小麦(Triticum aestivum)。该质粒包含几丁质酶和葡聚糖酶基因以及 nptII 基因作为选择性标记。几丁质酶和葡聚糖酶的表达分别由 CaMV35S 启动子和 Nos 终止子控制。从五个伊朗品种(Arta、Moghan、Sisun、Gascogen 和 A-Line)的种子中切取未成熟胚外植体,并在愈伤组织诱导培养基上培养以生成胚性愈伤组织。选择颜色浅奶油色和质地脆弱的胚性愈伤组织,并使用涂有重组 pBI-ChiGlu 质粒的金纳米颗粒进行轰击。轰击后的愈伤组织最初转移到选择性愈伤组织诱导培养基中,然后转移到选择性再生培养基中。两种培养基中的选择剂均为 25mg/L 的卡那霉素。在五个研究品种中,A-Line 的转化率最高(4.8%),其次是 Sisun、Gascogen 和 Arta。PCR 和 Southern blot 分析证实基因已整合到小麦品种的基因组中。此外,在体外试验中,使用来自转基因植物的 200μg 叶蛋白提取物显著抑制了禾谷镰刀菌的生长。根据我们的结果,与非转基因植物相比,转基因植物(T)表现出对镰刀菌的抗性。所有转基因植物均表现出正常的育性,在生长和发育过程中未观察到异常反应。