Affiliation:
1. International Cooperation Base of Science and Technology Innovation on Forest Resource Biotechnology, Central South University of Forestry and Technology, Changsha, China
2. Hunan Provincial Key Laboratory of Forestry Biotechnology, Central South University of Forestry and Technology, Changsha, China
3. Economic Forest Variety Creation Center, Yuelushan National Laboratory of Seed Industry, Changsha, China
Abstract
ABSTRACT
Glycerol dehydratase is the key and rate-limiting enzyme in the 1,3-propanediol synthesis pathway of
Klebsiella pneumoniae
, which determined the producing rate and yield of 1,3-propanediol. However, the expression regulation mechanism of glycerol dehydratase gene
dhaB
remains poorly unknown. In this study, a histone-like nucleoid-structuring (H-NS) protein was identified and characterized as the positive transcription regulator for
dhaB
expression in
K. pneumoniae
2e, which exhibited high tolerance against crude glycerol in our previous study. Deletion of
hns
gene significantly decreased the transcription level of
dhaB
in
K. pneumoniae
2e, which led to a remarkable defect on strain growth, glycerol dehydratase activity, and 3-hydroxypropanal production during glycerol fermentation. The transcription level of
dhaB
was significantly up-regulated in crude glycerol relative to pure glycerol, while the inactivation of H-NS resulted in more negative effect for transcription level of
dhaB
in the former. Though the H-NS expression level was almost comparable in both substrates, its multimer state was reduced in crude glycerol relative to pure glycerol, suggesting that the oligomerization state of H-NS might have contributed for positive regulation of
dhaB
expression. Furthermore, electrophoretic mobility shift and DNase I footprinting assays showed that H-NS could directly bind to the upstream promoter region of
dhaB
by recognizing the AT-rich region. These findings provided new insight into the transcriptional regulation mechanism of H-NS for glycerol dehydratase expression in
K. pneumoniae
, which might offer new target for engineering bacteria to industrially produce 1,3-propanediol.
IMPORTANCE
The biological production of 1,3-propanediol from glycerol by microbial fermentation shows great promising prospect on industrial application. Glycerol dehydratase catalyzes the penultimate step in glycerol metabolism and is regarded as one of the key and rate-limiting enzymes for 1,3-propanediol production. H-NS was reported as a pleiotropic modulator with negative effects on gene expression in most studies. Here, we reported for the first time that the expression of glycerol dehydratase gene is positively regulated by the H-NS. The results provide insight into a novel molecular mechanism of H-NS for positive regulation of glycerol dehydratase gene expression in
K. pneumoniae
, which holds promising potential for facilitating construction of engineering highly efficient 1,3-propanediol-producing strains.
Funder
MOST | National Natural Science Foundation of China
Science and Technology Program of Hunan Province
Key Scientific Research Project of Hunan Provincial Education Department
HSTD | Natural Science Foundation of Hunan Province
Program of Hunan Science and Technology Innovation Team
Publisher
American Society for Microbiology