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3-Hydroxypropionic acid (3-HP) and 1,3-propanediol (1,3-PDO) have tremendous potential markets in many industries. This study evaluated the simultaneous biosynthesis of the 2 compounds using the new psychrophile-based simple biocatalyst (PSCat) reaction system. The PSCat method is based on the expression of glycerol dehydratase, 1,3-propanediol dehydrogenase, and aldehyde dehydrogenase from Klebsiella pneumoniae in Shewanella livingstonensis Ac10 and Shewanella frigidimarina DSM 12253, individually. Heat treatment at 45 °C for 15 min deactivated the intracellular metabolic flux, and the production process was started after adding substrate, cofactor, and coenzyme. In the solo production process after 1 h, the maximum production of 3-HP was 62.0 m m. For 1,3-PDO, the maximum production was 25.0 m m. In the simultaneous production process, productivity was boosted, and the production of 3-HP and 1,3-PDO increased by 13.5 and 4.9 m m, respectively. Hence, the feasibility of the individual production and the simultaneous biosynthesis system were verified in the new PSCat approach.

1,3-Propanediol (1,3-PDO) is a valuable compound with a large potential market in many industries. This study aimed to evaluate the abilities of the Psychrophile-based Simple bioCatalyst (PSCat) reaction system to biosynthesize 1,3-PDO. This biocatalyst has a potential platform that replaces the chemical-based production counterparts. The two genes involved in the metabolic pathway were expressed both individually and together in the psychrophilic host bacterium. The intracellular metabolic flux was deactivated using heat treatment, at 45 °C for 15 min. After individual gene expression (25.0 mM), 1,3-PDO productivity of the cells increased by approximately 2.5 times, in comparison to when genes were expressed together (10.2 mM). Productivity was boosted (31.1 mM) when the cofactor regeneration system was activated in the biocatalyst. Hence, both the ability of individual gene expression and the cofactor regeneration system were verified in the PSCat approach. Nonetheless, further research is necessary to develop and optimize this process for industrial production.

In biopharmaceutical science, ion-exchange chromatography (IEC) is a well-known purification technique to separate the impurities such as host cell proteins from recombinant proteins. However, IEC is one of the limiting steps in the purification process of recombinant hepatitis B surface antigen (rHBsAg), due to its low recovery rate (

This study was carried out to isolate bacteria for bioremediation of petroleum polluted soils. Five samples were used for isolation in this study. They were four soil samples in addition to one kerosene sample. The soil samples including soils contaminated by crude oil and gas oil and two soil samples with no outward contamination which were collected from Shiraz Oil Refinery sites. Seven strains were selected among the isolated colonies for further experiments. The selected isolates were cultured in standard succinate medium (SSM) minimal medium in which 2.5% v/v kerosene was used as carbon source. In another bacterial SSM culture, carbon, sulfur or nitrogen source was removed and 20% v/v kerosene added to check the ability of isolates to utilizekerosene as sole source for C, N and S. Finally, cultures of four strains with higher growth in modified SSM cultures were selected for GC analysis. In this study they were named C2 and C4 which were isolated from crude oil contaminated soil and SI1 and SI2 isolated from soils with no outward contamination. GC analysis showed that C2 could degrade 69% of 5% v/v kerosene in 7 d, while C4 and SI1 degraded 48% and 42% of 5% v/v kerosene during this 7-d period respectively, and the degradation ability of SI2 was 38% after 7 d. Analysis of 16S rRNA gene showed that C2 was close to Citrobacter sedlakii, C4 and SI1 were related to Entrobacter hormeachei and SI2 was close to Entrobacter cloacae, respectively.