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Engineering self‐flocculating Halomonas campaniensis for wastewaterless open and continuous fermentation
Author(s) -
Ling Chen,
Qiao GuanQing,
Shuai BoWen,
Song KunNan,
Yao WenXi,
Jiang XiaoRan,
Chen GuoQiang
Publication year - 2019
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.26897
Subject(s) - halomonas , flocculation , fermentation , chemistry , aeration , bioreactor , food science , wastewater , industrial fermentation , chromatography , pulp and paper industry , biochemistry , environmental science , environmental engineering , organic chemistry , 16s ribosomal rna , engineering , gene
Halomonas has been developed as a platform for the next generation industrial biotechnology allowing open and nonsterile growth without microbial contamination under a high‐salt concentration and alkali pH. To reduce downstream cost associated with continuous centrifugation and salt containing wastewater treatment, Halomonas campaniensis strain LS21 was engineered to become self‐flocculating by knocking out an etf operon encoding two subunits of an electron transferring flavoprotein in the predicted electron transfer chain. Self‐flocculation could be attributed to the decrease of the surface charge and increase of the cellular hydrophobicity resulted from deleted etf . A wastewaterless fermentation strategy based on the self‐flocculating H. campaniensis was developed for growth and the production of poly‐3‐hydroxybutyrate (PHB) as an example. Most microbial cells flocculated and precipitated to the bottom of the bioreactor within 1 min after stopping the aeration and agitation. The supernatant can be used again without sterilization or inoculation for the growth of the next batch after collecting the precipitated cell mass. The wastewaterless process was conducted for four runs without generating wastewater. PHB accumulation by the self‐flocculent strain was enhanced via promoter and ribosome binding site optimizations, the productivities of cell dry weight and PHB were increased from 0.45 and 0.18 g·L −1 ·hr −1 for the batch process compared to 0.82 and 0.33 g·L −1 ·hr −1 for the wastewaterless continuous process, respectively. This has clearly demonstrated the advantages of the wastewaterless process in that it not only reduces wastewater but also increases cell growth and product formation efficiency in a given period of time.