Mycoprotein 2.0
Mycoprotein 2.0
批准号:
BB/P020364/1
负责人:
Richard Harrison
金额:
$68.77万
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2017
资助国家:
英国
项目状态:
已结题
起止时间:
2017 至 --
关键词:
中文摘要
随着繁荣程度的提高,对肉类的需求也会增加,因为它是一种丰富的蛋白质来源。这反过来又增加了对水资源的需求,改变了土地使用(在很大程度上取决于动物的喂养方式),并导致了人为温室气体排放的增加。一些国际机构已经确定,这是不可持续的,一些估计预计,到2050年,温室气体排放量占总排放量的比例将从目前的11%上升70%。然而,对蛋白质的需求也可以通过以作物为基础的来源(例如大豆和豆类)和真菌蛋白来满足,真菌蛋白是通过将作物衍生的葡萄糖发酵成生物质产生的,生物质被收获并加工成高质量的蛋白质。真菌蛋白在世界范围内仍然是一种相对未被开发的资源,但为全年生产高质量蛋白质提供了巨大的希望,这是未来粮食安全和人类营养的关键要求。生产面临的最大挑战是依赖单一的碳源,即小麦衍生的葡萄糖,它需要经过特殊处理才能适合使用。我们最近的工作表明,虽然用于产生真菌蛋白的真菌生长在这种葡萄糖底物上,但一些必需维生素的产生受到抑制。我们最近的工作揭示了维生素在一些其他碳源中的表达,例如甜菜提取的蔗糖糖浆。在某些情况下,但不是所有情况下,这与其他有害次生代谢物的增加有关。这就引出了一个问题,真菌是如何调节与碳源有关的次生代谢的?为了扩大真菌蛋白的营养价值和可利用的碳源范围(使生产转移到世界其他地区),我们将使用最新的DNA测序技术来揭示蛇毒镰刀菌基因组的结构,并研究基因组中包含次生代谢物基因的区域。从其他相关真菌的研究中得知,次生代谢(SM)的控制受SM簇在基因组中的位置和特定调控因子的调控。利用最新的测序技术将使我们能够定位SM位置并确定调节对不同碳源的反应的潜在机制。通过一系列受控批次和连续培养实验,我们将开发技术来选择性地诱导一系列碳源的维生素生物合成,而不会诱导有害SM基因的表达,从而为未来的产品开发提供对SM控制的理解和增强的产品。在已有工作的基础上,我们将扩展分子技术工具箱,以编辑毒藻基因组,去除有害的次生代谢物基因簇及其调控因子,这些基因簇是针对不同碳源诱导的。这项工作的结果是,利用更广泛的英国农业来源(玉米、大麦、水稻),将能够使用更广泛的碳源生产真菌蛋白,甚至转向以蔗糖为基础的真菌蛋白生产(一种目前完全无法获得的碳源),利用英国的蔗糖来源,如甜菜。此外,提高真菌蛋白中微量营养素补充量的能力将扩大其作为全球饮食的重要组成部分的效用,并提供一种更可持续和更灵活的肉类替代品。
英文摘要
As prosperity rises, demand for meat increases as it is a rich source of protein. This in turn places demand on water resources, changes land use (in a manner highly dependent upon how the animal is fed) and leads to an increase in anthropogenic GHG emissions. This has been determined to be unsustainable by a number of international bodies, with some estimates predicting a 70% rise from current levels of 11% of total GHG emissions by 2050. However, demand for protein can also be met by crop-based sources (e.g. soy and pulses) and by mycoprotein, produced by fermentation of crop-derived glucose into biomass, which is harvested and processed into high quality protein. Mycoprotein remains a relatively under-exploited resource worldwide but offers great promise for year-round production of high quality protein, a vital requirement for future food security and human nutrition. The most significant challenge to production is the reliance on a single carbon source, a wheat-derived glucose, which requires special processing before it is suitable for use. Our recent work has revealed that while the fungus used to produce mycoprotein is grown on this glucose substrate, production of a number of essential vitamins is inhibited. Our recent work has revealed that expression of vitamins in some other carbon sources, for example beet derived sucrose syrup is observed. In some, but not all cases, this is coupled to an increase in other deleterious secondary metabolites. This leads to the question, how is the fungus regulating secondary metabolism in relation to carbon source? To expand both the nutritional value of mycoprotein and the range of carbon sources that can be utilised (enabling production to move to other regions of the world) we will use the latest DNA sequencing techniques to reveal the structure of the genome of Fusarium venenatum and study the regions of the genome that contain secondary metabolite genes. From work carried out in other related fungi it is known that control of secondary metabolism (SM) is regulated by the position of SM cluster in the genome, and by specific regulatory factors. Utilising the latest sequencing techniques will allow us to positionally resolve SM location and determine the underlying mechanisms regulating responses to different carbon sources.Through a series of controlled batch and continuous culture experiments we will develop techniques to selectively induce vitamin biosynthesis across a range of carbon sources, without inducing the expression of deleterious SM genes, providing both an understanding of the control of SM and an enhanced product for future product development. Building on our existing work we will expand the toolbox of molecular techniques in order to edit the genome of F. venenatum to remove deleterious secondary metabolite gene clusters and their regulatory factors which are induced in response to different carbon sources. As a result of this work, mycoprotein will be able to be produced using a larger range of carbon sources drawing upon a wider range of UK agricultural sources (maize, barley, rice) and even shift to sucrose-based production of mycoprotein (a carbon source that has currently been completely inaccessible), utilising UK sources of sucrose such as sugar beet. Furthermore, the ability to enhance the complement of micronutrients in mycoprotein will broaden its utility as an important component of global diets and offers a more sustainable and flexible alternative to meat.
期刊论文(10)
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Additional file 6 of CRISPR/Cas9 mediated editing of the Quorn fungus Fusarium venenatum A3/5 by transient expression of Cas9 and sgRNAs targeting endogenous marker gene PKS12
CRISPR/Cas9 的附加文件 6 通过靶向内源标记基因 PKS12 的 Cas9 和 sgRNA 的瞬时表达介导 Quorn 真菌 Fusarium venenatum A3/5 的编辑
DOI:
10.6084/m9.figshare.17037354
发表时间:
2021
期刊:
影响因子:
--
作者:
[Wilson F]
通讯作者:
Wilson F
The Genome of the CTG(Ser1) Yeast Scheffersomyces stipitis Is Plastic.
CTG(SER1)酵母Scheffersomyces症状的基因组是塑料。
DOI:
10.1128/mbio.01871-21
发表时间:
2021-10-26
期刊:
mBio
影响因子:
6.4
作者:
[Vega-Estévez S, Armitage A, Bates HJ, Harrison RJ, Buscaino A]
通讯作者:
Buscaino A
Additional file 1 of CRISPR/Cas9 mediated editing of the Quorn fungus Fusarium venenatum A3/5 by transient expression of Cas9 and sgRNAs targeting endogenous marker gene PKS12
通过 Cas9 和 sgRNA 瞬时表达靶向内源标记基因 PKS12,CRISPR/Cas9 介导的 Quorn 真菌 Fusarium venenatum A3/5 编辑的附加文件 1
DOI:
10.6084/m9.figshare.17037333
发表时间:
2021
期刊:
影响因子:
--
作者:
[Wilson F]
通讯作者:
Wilson F
Additional file 8 of CRISPR/Cas9 mediated editing of the Quorn fungus Fusarium venenatum A3/5 by transient expression of Cas9 and sgRNAs targeting endogenous marker gene PKS12
CRISPR/Cas9 的附加文件 8 通过靶向内源标记基因 PKS12 的 Cas9 和 sgRNA 的瞬时表达介导 Quorn 真菌 Fusarium venenatum A3/5 的编辑
DOI:
10.6084/m9.figshare.17037363
发表时间:
2021
期刊:
影响因子:
--
作者:
[Wilson F]
通讯作者:
Wilson F
Additional file 2 of CRISPR/Cas9 mediated editing of the Quorn fungus Fusarium venenatum A3/5 by transient expression of Cas9 and sgRNAs targeting endogenous marker gene PKS12
通过 Cas9 和 sgRNA 瞬时表达靶向内源标记基因 PKS12,CRISPR/Cas9 介导的 Quorn 真菌 Fusarium venenatum A3/5 编辑的附加文件 2
DOI:
10.6084/m9.figshare.17037336
发表时间:
2021
期刊:
影响因子:
--
作者:
[Wilson F]
通讯作者:
Wilson F
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