4.7 Article

Revealing of sugar utilization systems in Halomonas sp. YLGW01 and application for poly(3-hydroxybutyrate) production with low-cost medium and easy recovery

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出版社

ELSEVIER
DOI: 10.1016/j.ijbiomac.2020.11.163

关键词

Poly(3-hydroxybutyrate); Halomonas; Whole genome sequencing; Carbon utilization; PHB microbead

资金

  1. National Research Foundation of Korea (NRF)s - Ministry of Science and ICT [2017M3A9E4077234]
  2. National Research Foundation of Korea (NRF) [NRF2019R1F1A1058805, 2015M3D3A1A01064882]
  3. R&D Program of MOTIE/KEIT [20009508]
  4. R&D Program for Forest Science Technology by Korea Forest Service (Korea Forestry Promotion Institute) [2020261C10-2022-AC02]
  5. Korea Forestry Promotion Institute (KOFPI) [2020261C10-2022-AC02] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2015M3D3A1A01064882] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Through deep-genome sequencing, key genes involved in PHB synthesis were identified in Halomonas sp. YLGW01, which demonstrated high-yield PHB production in a medium containing fructose in sea water.
Poly(3-hydroxybutyrate) (PHB) is a common polyhydroxyalkanoate (PHA) with potential as an alternative for petroleum-based plastics. Previously, we reported a new strain, Halomonas sp. YLGW01, which hyperproduces PHB with 94% yield using fructose. In this study, we examined the PHB production machinery of Halomonas sp. YLGW01 in more detail by deep-genome sequencing, which revealed a 3,453,067-bp genome with 65.1% guanine-cytosine content and 3054 genes. We found two acetyl-CoA acetyltransferases (Acetoacetyl-CoA thiolase, PhaA), one acetoacetyl-CoA reductase (PhaB), two PHB synthases (PhaC1, PhaC2), PHB depolymerase (PhaZ), and Enoyl-CoA hydratase (PhaJ) in the genome, alongwith two fructose kinases and fructose transporter systems, including the phosphotransferase system (PTS) and ATP-binding transport genes. We then examined the PHB production by Halomonas sp. YLGW01 using high-fructose corn syrup (HFCS) containing fructose, glucose, and sucrose in sea water medium, resulting in 7.95 +/- 0.11 g/L PHB (content, 67.39 +/- 0.34%). PHB was recovered from Halomonas sp. YLGW01 using different detergents; the use of Tween 20 and SDS yielded micro-sized granules with high purity. Overall, these results reveal the distribution of PHB synthetic genes and the sugar utilization system in Halomonas sp. YLGW01 and suggest a possible method for PHB recovery. (C) 2020 Elsevier B.V. All rights reserved.

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