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Characteristics of NtCCD1-3 from tobacco, and protein engineering of the CCD1 to enhance β-ionone production in yeast
Biosynthesis of β -ionone by microbial cell factories has become a promising way to obtain natural β -ionone. The catalytic activity of carotenoid cleavage dioxygenase 1 (CCD1) in cleavage of β -carotene to β -ionone severely limits its biosynthesis. In this study, NtCCD1-3 from Nicotiana tabacum wi...
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Published in: | Frontiers in microbiology 2022-09, Vol.13, p.1011297-1011297 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Biosynthesis of
β
-ionone by microbial cell factories has become a promising way to obtain natural
β
-ionone. The catalytic activity of carotenoid cleavage dioxygenase 1 (CCD1) in cleavage of
β
-carotene to
β
-ionone severely limits its biosynthesis. In this study, NtCCD1-3 from
Nicotiana tabacum
with high ability to cleave
β
-carotene was screened. Multiple strategies for improving the
β
-ionone yield in
Saccharomyces cerevisiae
were performed. The results showed that NtCCD1-3 could cleave a variety of caroteniods at the 9,10 (9′,10′) double bonds and lycopene at the 5,6 (5′,6′) positions. The insertion site delta for
NtCCD1-3
gene was more suitable for enhancing the yield of
β
-ionone, showing 19.1-fold increase compared with the rox1 site. More importantly, mutant K38A of NtCCD1-3 in membrane-bonding domains could greatly promote
β
-ionone production by more than 3-fold. We also found that overexpression of the NADH kinase Pos5 could improve
β
-ionone yield up to 1.5 times. These results may provide valuable references for biosynthesis of
β
-ionone. |
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ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2022.1011297 |