Screening of thermotolerant Gluconobacter strains for production of 5-keto-D-gluconic acid and disruption of flavin adenine dinucleotide-containing D-gluconate dehydrogenase
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Author list: Saichana I., Moonmangmee D., Adachi O., Matsushita K., Toyama H.
Publisher: American Society for Microbiology
Publication year: 2009
Journal: Applied and Environmental Microbiology (0099-2240)
Volume number: 75
Issue number: 13
Start page: 4240
End page: 4247
Number of pages: 8
ISSN: 0099-2240
eISSN: 1098-5336
Languages: English-Great Britain (EN-GB)
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Abstract
We isolated thermotolerant Gluconobacter strains that are able to produce 5-keto-D-gluconic acid (5KGA) at 37ฐC, a temperature at which regular mesophilic 5KGA-producing strains showed much less growth and 5KGA production. The thermotolerant strains produced 2KGA as the major product at both 30 and 37ฐC. The amount of ketogluconates produced at 37ฐC was slightly less than the amount produced at 30ฐC. To improve the yield of 5KGA in these strains, we disrupted flavin adenine dinucleotide-gluconate dehydrogenase (FAD-GADH), which is responsible for 2KGA production. Genes for FAD-GADH were cloned by using inverse PCR and an in vitro cloning strategy. The sequences obtained for three thermotolerant strains were identical and showed high levels of identity to the FAD-GADH sequence reported for the genome of Gluconobacter oxydans 621 H. A kanamycin resistance gene cassette was used to disrupt the FAD-GADH genes in the thermotolerant strains. The mutant strains produced 5KGA exclusively, and the final yields were over 90% at 30ฐC and 50% at 37ฐC. We found that the activity of pyrroloquinoline quinone (PQQ)-dependent glycerol dehydrogenase, which is responsible for 5KGA production, increased in response to addition of PQQ and CaCl2 in vitro when cells were grown at 37ฐC. Addition of 5 mM CaCl2 to the culture medium of the mutant strains increased 5KGA production to the point where over 90% of the initial substrate was converted. The thermotolerant Gluconobacter strains that we isolated in this study provide a promising new option for industrial 5KGA production. Copyright ฉ 2009, American Society for Microbiology. All Rights Reserved.
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