Department of Chemical Engineering, University of California at Davis, Davis, CA, 95616, USA.
Appl Microbiol Biotechnol. 2017 Jun;101(12):4895-4903. doi: 10.1007/s00253-017-8241-5. Epub 2017 Mar 29.
Production of recombinant proteins in plants through Agrobacterium-mediated transient expression is a promising method of producing human therapeutic proteins, vaccines, and commercial enzymes. This process has been shown to be viable at a large scale and involves growing large quantities of wild-type plants and infiltrating the leaf tissue with a suspension of Agrobacterium tumefaciens bearing the genes of interest. This study examined one of the steps in this process that had not yet been optimized: the scale-up of Agrobacterium production to sufficient volumes for large-scale plant infiltration. Production of Agrobacterium strain C58C1 pTFS40 was scaled up from shake flasks (50-100 mL) to benchtop (5 L) scale with three types of media: Lysogeny broth (LB), yeast extract peptone (YEP) media, and a sucrose-based defined media. The maximum specific growth rate (μ ) of the strain in the three types of media was 0.46 ± 0.04 h in LB media, 0.43 ± 0.03 h in YEP media, and 0.27 ± 0.01 h in defined media. The maximum biomass concentration reached at this scale was 2.0 ± 0.1, 2.8 ± 0.1, and 2.6 ± 0.1 g dry cell weight (DCW)/L for the three media types. Production was successfully scaled up to a 100-L working volume reactor with YEP media, using k a as the scale-up parameter.
通过农杆菌介导的瞬时表达在植物中生产重组蛋白是生产人治疗性蛋白、疫苗和商业酶的一种很有前途的方法。该方法已被证明在大规模生产中是可行的,涉及到大量野生型植物的生长和用携带感兴趣基因的农杆菌悬浮液浸润叶片组织。本研究考察了该过程中尚未优化的步骤之一:将农杆菌生产扩大到足以进行大规模植物浸润的规模。农杆菌菌株 C58C1 pTFS40 的生产从摇瓶(50-100 mL)扩大到台式(5 L)规模,使用了三种培养基:LB 培养基、酵母提取物-蛋白胨(YEP)培养基和基于蔗糖的定义培养基。在三种培养基中,该菌株的最大比生长速率(μ)在 LB 培养基中为 0.46±0.04 h,在 YEP 培养基中为 0.43±0.03 h,在定义培养基中为 0.27±0.01 h。在该规模下达到的最大生物量浓度分别为三种培养基类型的 2.0±0.1、2.8±0.1 和 2.6±0.1 g 干细胞重量(DCW)/L。使用 k a 作为放大参数,成功地将 YEP 培养基放大到 100-L 工作体积的反应器中。