双奖杯微管生物膜反应器规模扩大的第一步-防止生物膜脱离

Biofilms Pub Date : 2020-07-01 DOI:10.5194/biofilms9-13
A. Kenkel, Andreas Schmid, R. Karande, Katja Bühler
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引用次数: 0

摘要

光养蓝细菌在生物技术中的应用非常有趣,因为它们代表了一个碳中和的生产平台,主要依靠二氧化碳、光和水进行生长。然而,利用蓝藻作为生产宿主的一个关键瓶颈是,在目前建立的培养系统(如管式或平板反应器)中,只有2至4gCDW/L的细胞密度是可能的,这对于大多数应用来说至少低了20倍。解决这一缺点的一个很有前途的概念是在微管系统中以带有气泡的分段流动方式培养这种微生物,如双奖杯生物膜,正如最近在[1]中报道的那样。根据Posten等人[2]中提到的方面,很明显,该概念满足了光生物反应器的大多数要求。首先,表面积与体积比随着管径的减小而增大。因此,光通过反应器的路径减少,从而导致最佳的光供应。其次,使用空气段增加了反应器内的混合,从而更好地为电池提供碳源以及更好地提取氧气。除此之外,附着的生物膜提供连续的细胞再生,从而提供连续的生产系统。所有这些方面导致该反应器系统中的生物质浓度高达60gCDW/L[1]。微管系统成功应用于环己烷转化为环己醇的挑战性转化[1]。该反应是在一个小型实验室规模的系统中进行的,该系统利用20厘米长、总体积为1.4毫升的毛细管。在这里,我们正在评估更大规模对生物膜性能的影响。实验在内径为3mm的1m毛细管中进行。首先,研究了不同流速的影响。结果表明;L/分钟(52×L空气和52×L培养基/分钟)导致培养一周后管中不同位置的生物膜显著脱离。总流量为520;L/分钟(260µ;L空气和260µ!L介质/分钟)防止分离,然而,它似乎阻碍了管的完全表面覆盖。结果证明,最佳条件是以520°的起始流速培养生物膜;L/分钟,用于细胞的初始附着和流量连续降低到104;培养一周后L/分钟。从而防止了生物膜分离,并实现了完全的表面覆盖,同时将系统缩放5倍。将介绍和讨论各自的数据。[1] Hoschek,Heuschkel,用于Synechocystis sp.PCC 6803在毛细管反应器中连续环己烷氧化为环己醇的高细胞密度应用的混合物种生物膜,生物资源技术,2019[2]Posten,微藻培养用光生物反应器的设计原理,生命科学工程,2009
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First steps for the scale up of a dual trophies microtubular biofilm reactor - preventing biofilm detachment

The use of phototrophic cyanobacteria in biotechnology is highly interesting as they represent a carbon neutral production platform, relying mainly on carbon dioxide, light and water for growth. However, one key bottleneck for utilizing cyanobacteria as production hosts is that in the currently established cultivation systems like tube or flatpanel reactors only cell densities of 2 to 4 gCDW/L are possible, which is at least 20 times too low for most applications. One promising concept to solve this shortcoming is the cultivation of such microbes as dual trophies biofilms in microtubular systems in a segmented flow fashion with air bubbles, as recently reported in [1]. According to the aspects mentioned in Posten et. al [2], it becomes clear that the concept fulfils most requirements for photo-bioreactors. Firstly, the surface area to volume ratio is increasing with decreasing tube diameter. Hence, the path of the light through the reactor is reduced, leading to an optimal light supply. Secondly, using air segments increases the mixing within the reactor leading to a better supply of the cells with a carbon source as well as a better extraction of oxygen. Apart from that, the attached biofilm provides continuous cell regeneration and thus a continuous production system. All these aspects lead to a biomass concentration in this reactor system of up to 60 gCDW/L [1].

The microtubular system was successfully applied in the challenging conversion of cyclohexane to cyclohexanol [1]. The reaction was conducted in a small lab scale system utilizing capillaries of 20 cm length, with a total volume of 1.4 mL. Here, we are evaluating the impact of larger scale on biofilm performance. Experiments were conducted in 1 m capillaries with 3 mm inner diameter. First, the impact of different flow rates was investigated. Results show, that a total minimal flow rate of 104 µL/min (52 µL air and 52 µL medium /min) leads to a significant biofilm detachment in various positions in the tube after one week of cultivation. A total flow rate of 520 µL/min (260 µL air and 260 µL medium /min) prevents detachment, however, it seems to hinder full surface coverage of the tube. An optimal condition turned out to be a cultivation of the biofilm with a starting flowrate of 520 µL/min for the initial attachment of the cells and a consecutive decrease of the flow to 104 µL/min after one week of cultivation. Thereby biofilm detachment was prevented and full surface coverage was achieved, while scaling the system by 5 fold. Respective data will be presented and discussed.

[1] Hoschek, Heuschkel, Mixed-species biofilms for high-cell-density application of Synechocystis sp. PCC 6803 in capillary reactors for continuous cyclohexane oxidation to cyclohexanol, Bioresource Technology, 2019

[2] Posten, Design principles of photo-bioreactors for cultivation of microalgae, Engineering in Life Sciences, 2009

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