4.6 Article

Improved enzyme production by bio-pellets of Aspergillus niger: Targeted morphology engineering using titanate microparticles

Journal

BIOTECHNOLOGY AND BIOENGINEERING
Volume 109, Issue 2, Pages 462-471

Publisher

WILEY-BLACKWELL
DOI: 10.1002/bit.23313

Keywords

morphology engineering; core shell pellet; filamentous fungi; critical pellet diameter; fructofuranosidase; glucoamylase

Funding

  1. German Research Foundation (DFG) [B11]

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The present study describes the design of bio-pellet morphologies of the industrial working horse Aspergillus niger strains in submerged culture. The novel approach recruits the intended addition of titanate microparticles (TiSiO4, 8?mu mu m) to the growth medium. As tested for two recombinant strains producing fructofuranosidase and glucoamylase, the enzyme titer by the titanate-enhanced cultures in shake flasks was increased 3.7-fold to 150?U/mL (for fructofuranosidase) and 9.5-fold to 190?U/mL (for glucoamylase) as compared to the control. This could be successfully utilized for improved enzyme production in stirred tank reactors. Stimulated by the particles, the achieved final glucoamylase activity of 1,080?U/mL (fed-batch) and 320?U/mL (batch) was sevenfold higher as compared to the conventional processes. The major reason for the enhanced production was the close association between the titanate particles and the fungal cells. Already below 2.5?g/L the micromaterial was found inside the pellets, including single particles embedded as 50150?mu m particle aggregates in the center resulting in core shell pellets. With increasing titanate levels the pellet size decreased from 1,700?mu m (control) to 300?mu m. Fluorescence based resolution of GFP expression revealed that the large pellets of the control were only active in a 200?mu m surface layer. This matches with the critical penetration depth for nutrients and oxygen typically observed for fungal pellets. The biomass within the titanate derived fungal pellets, however, was completely active. This was due a reduced thickness of the biomass layer via smaller pellets as well as the core shell structure. Moreover, also the created loose inner pellet structure enabled a higher mass transfer and penetration depths for up to 500?mu m. The creation of core-shell pellets has not been achieved previously by the addition of microparticles, for example, made of talc or alumina. Due to this, the present work opens further possibilities to use microparticles for tailor-made morphology design of filamentous fungi, especially for pellet based processes which have a long and strong industrial relevance for industrial production. Biotechnol. Bioeng. 2012; 109:462471. (c) 2011 Wiley Periodicals, Inc.

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