4.7 Article

Relationship between β-D-fructofuranosidase activity, fructooligosaccharides and pullulan biosynthesis in Aureobasidium melanogenum P16

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 125, Issue -, Pages 1103-1111

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijbiomac.2018.12.141

Keywords

beta-D-fructofuranosidase; Fructooligosaccharides; Pullulan; Aureobasidium melanogenum; Transcriptional activator

Funding

  1. National Natural Science Foundation of China [31770061]

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It has been thought that when different strains of Aureobasidium spp. were grown in sucrose, the produced fructooligosaccharides (FOSs) by beta-D-fructofuranosidase were beneficial for their cell growth and pullulan biosynthesis. However, it is still unknown about how beta-D-fructofuranosidases activity and synthesized FOSs influence on pullulan biosynthesis. It was found that the genomic DNA of Aureobasidium melanogenum P16, a high pullulan producing yeast, contained three genes encoding beta-D-fructofuranosidase1, beta-D-fructofuranosidase2 and beta-D-fructofuranosidase3. The FTR1 factor, a transcriptional activator, activated expression of the three beta-D-fructofuranosidase genes and invertase gene. Disruption of the FTR1 gene rendered a disruptant DF3 to produce less FOSs (12.1 +/- 0.4 g/L), less beta-D-fructofuranosidase activity (1.1 +/- 0.2 U/mL), lower Mw (3.8 x 10 (5)) of the pullulan and more pullulan titer (77.0 +/- 2.6 g/L) than the yeast strain P16. Similarly, removal of both the two genes encoding beta-D-fructofuranosidase1 and beta-D-fructofuranosidase3 resulted in a double mutant DF4-7 producing 77.5 +/- 3.1 g/L pullulan with Mw of 3.4 x 10 (5), 0.2 +/- 0.0 U/mL of beta-D-fructofuranosidase activity and the trace amount of FOSs while its wild type strain P16 yielded 65.7 +/- 3.5 g/L pullulan with Mw of 4.4 x 10 (5), 6.8 +/- 0.0 U/mL of beta-D-fructofuranosidase activity and 6.2 +/- 0.5 g/L of FOSs. These confirmed that high beta-D-fructofuranosidase activity, the presence of high level of FOSs negatively influenced pullulan biosynthesis, but positively increased Mw of the produced pullulan. However, the beta-D-fructofuranosidase2 had no such function. Furthermore, complementation of the FTR1 gene, beta-D-fructofuranosidase1 gene and beta-D-fructofuranosidase3 gene enabled the corresponding transformants to restore beta-D-fructofuranosidase activity, FOSs and pullulan biosynthesis and Mw of the pullulan. (C) 2018 Elsevier B.V. All rights reserved.

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