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Comparative proteomic analyses of Hyphozyma roseonigra ATCC 20624 in response to sclareol. | LitMetric

AI Article Synopsis

  • - Sclareol is a key intermediate in the production of ambroxide, and the strain Hyphozyma roseonigra ATCC 20624 is the only known organism capable of breaking it down into sclareol glycol, which is vital for ambroxide synthesis.
  • - Researchers conducted proteomic analyses to see how H. roseonigra reacts to sclareol compared to glucose, identifying 79 protein spots that were significantly upregulated under sclareol conditions.
  • - Of the proteins identified, many are linked to metabolism and cellular processes, with eighteen specifically being aldehyde dehydrogenases, suggesting their crucial role in sclareol metabolism and paving the way for better production strategies for sclareol glycol.*

Article Abstract

Sclareol is an important intermediate for ambroxide synthesis industries. Hyphozyma roseonigra ATCC 20624 was the only reported strain capable of degrading sclareol to the main product of sclareol glycol, which is the precursor of ambroxide. To date, knowledge is lacking about the effects of sclareol on cells and the proteins involved in sclareol metabolism. Comparative proteomic analyses were conducted on the strain H. roseonigra ATCC 20624 by using sclareol or glucose as the sole carbon source. A total of 79 upregulated protein spots with a > 2.0-fold difference in abundance on 2-D gels under sclareol stress conditions were collected for further identification. Seventy spots were successfully identified and finally integrated into 30 proteins. The upregulated proteins under sclareol stress are involved in carbon metabolism and nitrogen metabolism, and replication, transcription, and translation processes. Eighteen upregulated spots were identified as aldehyde dehydrogenases, which indicating that aldehyde dehydrogenases might play an important role in sclareol metabolism. Overall, this study may lay the fundamentals for further cell engineering to improve sclareol glycol production.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863283PMC
http://dx.doi.org/10.1007/s42770-019-00040-2DOI Listing

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