Co-overexpression of chitinase and β-1,3-glucanase significantly enhanced the resistance of Iranian wheat cultivars to Fusarium.

IF 3.5 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Negin Mohammadizadeh-Heydari, Masoud Tohidfar, Bahram Maleki Zanjani, Motahhareh Mohsenpour, Rahele Ghanbari Moheb Seraj, Keyvan Esmaeilzadeh-Salestani
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引用次数: 0

Abstract

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 (T1) 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.

几丁质酶和β-1,3-葡聚糖酶的共重表达显著增强了伊朗小麦品种对镰刀菌的抗性。
镰刀菌头孢疫病(FHB)是一种毁灭性真菌疾病,影响不同谷物,尤其是小麦,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,它们以几丁质和β-葡聚糖微纤维等重要的大分子成分为靶标,参与裂解真菌细胞壁。在我们的实验中,使用生物技术和重组 pBI121 质粒(pBI-ChiGlu (-))引入几丁质酶和葡聚糖酶基因,产生了转基因小麦(Triticum aestivum)。该质粒含有几丁质酶和葡聚糖酶基因以及作为可选择标记的 nptII 基因。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。从五个伊朗栽培品种(Arta、Moghan、Sisun、Gascogen 和 A-Line)的种子上切除未成熟胚外植体,并在胼胝体诱导培养基上培养以产生胚性胼胝体。选取颜色为浅奶油色、质地较脆的胚胎茧,使用涂有重组 pBI-ChiGlu 质粒的金纳米粒子进行轰击。轰炸后的胼胝体先转移到选择性胼胝体诱导培养基上,然后再转移到选择性再生培养基上。两种培养基中的卡那霉素浓度均为 25 毫克/升。在研究的五个栽培品种中,A-Line 的转化率最高(4.8%),其次依次是 Sisun、Gascogen 和 Arta。聚合酶链式反应和 Southern 印迹分析证实了小麦栽培品种基因组中的整合基因。此外,在体外试验中,使用 200 μg 的转基因植株叶蛋白提取物可显著抑制禾本科镰刀菌的生长。结果表明,与非转基因植物相比,转基因植物(T1)对镰刀菌具有抗性。所有转基因植株的生育力均正常,生长发育也未出现异常反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Biotechnology
BMC Biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.60
自引率
0.00%
发文量
34
审稿时长
2 months
期刊介绍: BMC Biotechnology is an open access, peer-reviewed journal that considers articles on the manipulation of biological macromolecules or organisms for use in experimental procedures, cellular and tissue engineering or in the pharmaceutical, agricultural biotechnology and allied industries.
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