4.6 Article

Constitutive Expression in Komagataella phaffii of Mature Rhizopus oryzae Lipase Jointly with Its Truncated Prosequence Improves Production and the Biocatalyst Operational Stability

Journal

CATALYSTS
Volume 11, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/catal11101192

Keywords

Rhizopus oryzae lipase; Komagataella phaffii; prosequence; flavor; biodiesel; biocatalysis

Funding

  1. Spanish Ministry of Science and Innovation [PID2019104666GB-100]

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In this study, the Rhizopus oryzae lipase (ROL) with a 27-amino acid prosequence was successfully expressed in Komagataella phaffii, resulting in significantly higher activity and productivity compared to methanol-induced expression. The truncated prosequence enabled more efficient production of proROL and the immobilized form showed increased stability in biodiesel and ethyl butyrate production processes.
Rhizopus oryzae lipase (ROL) containing 28 C-terminal amino acids of the prosequence fused to the N-terminal mature sequence in ROL (proROL) was successfully expressed in the methylotrophic yeast Komagataella phaffii (Pichia pastoris) under the constitutive glyceraldehyde-3-phosphate dehydrogenase promoter (P-GAP). Although the sequence encoding the mature lipase (rROL) was also transformed, no clones were obtained after three transformation cycles, which highlights the importance of the truncated prosequence to obtain viable transformed clones. Batch cultures of the K. phaffii strain constitutively expressing proROL scarcely influenced growth rate and exhibited a final activity and volumetric productivity more than six times higher than those obtained with proROL from K. phaffii under the methanol-inducible alcohol oxidase 1 promoter (P-AOX1). The previous differences were less marked in fed-batch cultures. N-terminal analysis confirmed the presence of the 28 amino acids in proROL. In addition, immobilized proROL exhibited increased tolerance of organic solvents and an operational stability 0.25 and 3 times higher than that of immobilized rROL in biodiesel and ethyl butyrate production, respectively. Therefore, the truncated prosequence enables constitutive proROL production, boosts bioprocess performance and provides a more stable biocatalyst in two reactions in which lipases are mostly used at industrial level, esterification (ethyl butyrate) and transesterification (biodiesel).

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