平行生物反应器策略快速确定生物生产的生长耦合关系:甲羟戊酸案例研究

IF 6.1 1区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology for Biofuels Pub Date : 2025-01-17 DOI:10.1186/s13068-024-02599-x
Alec Banner, Joseph Webb, Nigel Scrutton
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引用次数: 0

摘要

气候危机和日益枯竭的化石燃料储备已经推动了“绿色”替代我们制造化学品的方式,并形成了一种生物经济,减少了我们对石化原料的依赖。合成生物学的进步为设计微生物从可再生原料中生产化合物提供了机会,这可能在取代传统的、基于石化的制造路线方面发挥作用。然而,很少有生物制造产品实现商业化的例子。这可能部分是由于学术和工业重点之间的差异,需要在较早阶段更加强调经济可行性。萜类化合物是一类在燃料、材料和制药工业中具有多种用途的化合物,可以从关键的中间体甲羟戊酸生物合成。在这里,我们报告了一种利用平行生物反应器快速绘制特定产物形成速率、特定底物利用率和特定生长速率之间的生长耦合关系的方法。以甲羟戊酸为例,在生长速率(\(\mu\))为0.34 h−1的条件下,最大产率系数为0.18 gp/gs。然而,这一过程也导致了有毒副产品醋酸盐的形成,醋酸盐会减缓生长,并在下游加工过程中造成问题。通过基因编辑敲除大肠杆菌BW25113中的ackA-pta操纵子和poxB,我们能够在不形成乙酸的情况下获得相同的最佳产率。结论采用平行生物反应器评价甲羟戊酸生产效率的有效性,以及生长速率与产率系数之间的耦合关系。利用基因工程技术,我们得到的菌株显示出甲羟戊酸的快速形成,没有不需要的副产品醋酸盐。甲羟戊酸的生产是量化的,并以工业相关单位报告,包括转换效率等关键参数,这些参数在早期的出版物中经常被省略,报告的滴度仅为g/L。
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A parallel bioreactor strategy to rapidly determine growth-coupling relationships for bioproduction: a mevalonate case study

Background

The climate crisis and depleting fossil fuel reserves have led to a drive for ‘green’ alternatives to the way we manufacture chemicals, and the formation of a bioeconomy that reduces our reliance on petrochemical-based feedstocks. Advances in Synthetic biology have provided the opportunity to engineer micro-organisms to produce compounds from renewable feedstocks, which could play a role in replacing traditional, petrochemical based, manufacturing routes. However, there are few examples of bio-manufactured products achieving commercialisation. This may be partially due to a disparity between academic and industrial focus, and a greater emphasis needs to be placed on economic feasibility at an earlier stage. Terpenoids are a class of compounds with diverse use across fuel, materials and pharmaceutical industries and can be manufactured biologically from the key intermediate mevalonate.

Results

Here, we report on a method of utilising parallel bioreactors to rapidly map the growth-coupling relationship between the specific product formation rate, specific substrate utilisation rate and specific growth rate. Using mevalonate as an example product, a maximum product yield coefficient of 0.18 gp/gs was achieved at a growth rate (\(\mu\)) of 0.34 h−1. However, this process also led to the formation of the toxic byproduct acetate, which can slow growth and cause problems during downstream processing. By using gene editing to knock out the ackA-pta operon and poxB from E. coli BW25113, we were able to achieve the same optimum production rate, without the formation of acetate.

Conclusions

We demonstrated the power of using parallel bioreactors to assess productivity and the growth-coupling relationship between growth rate and product yield coefficient of mevalonate production. Using genetic engineering, our resultant strain demonstrated rapid mevalonate formation without the unwanted byproduct acetate. Mevalonate production is quantified and reported in industrially relevant units, including key parameters like conversion efficiency that are often omitted in early-stage publications reporting only titre in g/L.

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来源期刊
Biotechnology for Biofuels
Biotechnology for Biofuels 工程技术-生物工程与应用微生物
自引率
0.00%
发文量
0
审稿时长
2.7 months
期刊介绍: Biotechnology for Biofuels is an open access peer-reviewed journal featuring high-quality studies describing technological and operational advances in the production of biofuels, chemicals and other bioproducts. The journal emphasizes understanding and advancing the application of biotechnology and synergistic operations to improve plants and biological conversion systems for the biological production of these products from biomass, intermediates derived from biomass, or CO2, as well as upstream or downstream operations that are integral to biological conversion of biomass. Biotechnology for Biofuels focuses on the following areas: • Development of terrestrial plant feedstocks • Development of algal feedstocks • Biomass pretreatment, fractionation and extraction for biological conversion • Enzyme engineering, production and analysis • Bacterial genetics, physiology and metabolic engineering • Fungal/yeast genetics, physiology and metabolic engineering • Fermentation, biocatalytic conversion and reaction dynamics • Biological production of chemicals and bioproducts from biomass • Anaerobic digestion, biohydrogen and bioelectricity • Bioprocess integration, techno-economic analysis, modelling and policy • Life cycle assessment and environmental impact analysis
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