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Development of bicistronic expression system for the enhanced and reliable production of recombinant proteins in Leuconostoc citreum
The lactic acid bacteria (LAB) Leuconostoc citreum are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in L . citreum , we developed a bicistronic design (BCD) exp...
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Published in: | Scientific reports 2018-06, Vol.8 (1), p.8852-11, Article 8852 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The lactic acid bacteria (LAB)
Leuconostoc citreum
are non-sporulating hetero-fermentative bacteria that play an important role in the fermented food industry. In this study, for the enhanced and reliable production of recombinant proteins in
L
.
citreum
, we developed a bicistronic design (BCD) expression system which includes a short leader peptide (1
st
cistron) followed by target genes (2
nd
cistron) under the control of a single promoter. Using superfolder green fluorescent protein (sfGFP) as a reporter, the functionality of BCD in
L
.
citreum
was verified. Further, to improve the expression in BCD, we tried to engineer a Shine-Dalgarno sequence (SD2) for the 2
nd
cistron and a promoter by FACS screening of random libraries, and both strong SD2 (eSD2) and promoter (P
710V4
) were successfully isolated. The usefulness of the engineered BCD with P
710V4
and eSD2 was further validated using three model proteins—glutathione-s-transferase, human growth hormone, and α-amylase. All examined proteins were successfully produced with levels highly increased compared with those in the original BCD as well as the monocistronic design (MCD) expression system. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-018-27091-z |