Division of Biotechnology and Plant Health, Norwegian Institute of Bioeconomy Research (NIBIO), P.O. Box 115, NO-1431 Ås, Norway.
Division of Biotechnology and Plant Health, Norwegian Institute of Bioeconomy Research (NIBIO), P.O. Box 115, NO-1431 Ås, Norway.
Int J Food Microbiol. 2020 Oct 16;331:108712. doi: 10.1016/j.ijfoodmicro.2020.108712. Epub 2020 Jun 2.
The bread-making quality of wheat depends on the viscoelastic properties of the dough in which gluten proteins play an important role. The quality of gluten proteins is influenced by the genetics of the different wheat varieties and environmental factors. Occasionally, a near complete loss of gluten strength, measured as the maximum resistance towards stretching (R), is observed in grain lots of Norwegian wheat. It is hypothesized that the loss of gluten quality is caused by degradation of gluten proteins by fungal proteases. To identify fungi associated with loss of gluten strength, samples from a selection of wheat grain lots with weak gluten (n = 10, R < 0.3 N) and strong gluten (n = 10, R ≥ 0.6 N) was analyzed for the abundance of fungal operational taxonomic units (OTUs) using DNA metabarcoding of the nuclear ribosomal Internal Transcribed Spacer (ITS) region ITS1. The DNA quantities for a selection of fungal pathogens of wheat, and the total amount of fungal DNA, were analyzed by quantitative PCR (qPCR). The mean level of total fungal DNA was higher in grain samples with weak gluten compared to grain samples with strong gluten. Heightened quantities of DNA from fungi within the Fusarium Head Blight (FHB) complex, i.e. Fusarium avenaceum, Fusarium graminearum, Microdochium majus, and Microdochium nivale, were observed in grain samples with weak gluten compared to those with strong gluten. Microdochium majus was the dominant fungus in the samples with weak gluten. Stepwise regression modeling based on different wheat quality parameters, qPCR data, and the 35 most common OTUs revealed a significant negative association between gluten strength and three OTUs, of which the OTU identified as M. majus was the most abundant. The same analysis also revealed a significant negative relationship between gluten strength and F. avenaceum detected by qPCR, although the DNA levels of this fungus were low compared to those of M. majus. In vitro growth rate studies of a selection of FHB species showed that all the tested isolates were able to grow with gluten as a sole nitrogen source. In addition, proteins secreted by these fungi in liquid cultures were able to hydrolyze gluten substrate proteins in zymograms, confirming their capacity to secrete gluten-degrading proteases. The identification of fungi with potential to influence gluten quality can enable the development of strategies to minimize future problems with gluten strength in food-grade wheat.
小麦的面包制作质量取决于面团的黏弹性,其中谷蛋白起到了重要作用。谷蛋白的质量受到不同小麦品种遗传和环境因素的影响。偶尔,在挪威小麦的一批谷物中,会观察到谷朊强度近乎完全丧失,其表现为拉伸阻力(R)的最大值。据推测,谷朊质量的损失是由真菌蛋白酶对谷蛋白的降解引起的。为了确定与谷朊强度丧失相关的真菌,对选择的一批弱筋小麦(n=10,R<0.3 N)和强筋小麦(n=10,R≥0.6 N)的样品进行了基于核核糖体内部转录间隔区(ITS)ITS1 的 DNA 元条形码的真菌分类单元(OTU)丰度分析。通过定量 PCR(qPCR)分析了小麦的一些真菌病原体和总真菌 DNA 的 DNA 量。与强筋小麦相比,弱筋小麦的总真菌 DNA 含量更高。与强筋小麦相比,在弱筋小麦中观察到真菌镰刀菌头疫病(FHB)复合体,即禾谷镰刀菌、小麦赤霉、大丽轮枝菌和禾谷镰孢菌的 DNA 量增加。在弱筋小麦样品中,大丽轮枝菌是优势真菌。基于不同小麦质量参数、qPCR 数据和 35 个最常见 OTU 的逐步回归模型表明,谷朊强度与三个 OTU 呈显著负相关,其中鉴定为大丽轮枝菌的 OTU 是最丰富的。同样的分析还表明,谷朊强度与 qPCR 检测到的禾谷镰刀菌呈显著负相关,尽管该真菌的 DNA 水平低于大丽轮枝菌。对一些 FHB 种的选择进行体外生长速率研究表明,所有测试的分离株都能够以谷朊作为唯一氮源进行生长。此外,这些真菌在液体培养中分泌的蛋白质能够在同工酶中水解谷朊底物蛋白,证实了它们分泌谷朊降解蛋白酶的能力。鉴定出具有影响谷朊质量潜力的真菌,可以为制定策略以最小化未来食品级小麦中谷朊强度问题提供帮助。