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A kinetic model to optimize and direct the dose ratio of Dsz enzymes in the 4S desulfurization pathway in vitro and in vivo

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Abstract

Objective

To enhance the biodesulfurization rate using a kinetic model that directs the ratio of Dsz enzymes.

Results

This study established a kinetic model that predicted the optimal ratio of Dsz enzymes in the 4S biodesulfurization system to be A:B:C = 1:2:4 and 1:4:2. When BCAD+1A+4B+2C, the conversion rate of dibenzothiophene (DBT) to 2-hydroxybiphenyl (HBP) was close to 100% in vitro. When the gene dose of dszC was increased, the HBP yield of the recombinant strain BL21(DE3)/BCAD + C reached approximately 0.012 mM in vivo, which was approximately 6-fold higher than that of the BCAD strain.

Conclusions

According to the results predicted by the enzyme kinetic model, maintaining higher concentrations of DszC and DszB in the desulfurization system can effectively improve the desulfurization efficiency.

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Abbreviations

HDS:

Hydrodesulfurization

BDS:

Biodesulfurization

DBT:

Dibenzothiophene

HBP:

2-Hydroxybiphenyl

DBTO2 :

Dibenzothiophene sulfone

HBPS:

2-(2-Hydroxybiphenyl) 2 sulfinic acid salt

HPLC:

High-performance liquid chromatography

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Supporting information

Supplementary Figure 1. The rate of conversion of DBT to HBP by BL21(DE3)/BADC+C.

Funding

This research was financially supported by the National Natural Science Foundation of China (Grant No. 31470159), the National Science Foundation for Young Scientists of China (Grant No. 31400062).

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Correspondence to Ying Lin or Shuli Liang.

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The authors declare no competing financial interest.

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Li, L., Ye, L., Guo, Z. et al. A kinetic model to optimize and direct the dose ratio of Dsz enzymes in the 4S desulfurization pathway in vitro and in vivo. Biotechnol Lett 41, 1333–1341 (2019). https://doi.org/10.1007/s10529-019-02730-1

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  • DOI: https://doi.org/10.1007/s10529-019-02730-1

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