Publications by authors named "Pietro Butti"

Background: The textile industry has several negative impacts, mainly because it is based on a linear business model that depletes natural resources and produces excessive amounts of waste. Globally, about 75% of textile waste is disposed of in landfills and only 25% is reused or recycled, while less than 1% is recycled back into new garments. In this study, we explored the valorisation of cotton fabric waste from an apparel textile manufacturing company as valuable biomass to produce lactic acid, a versatile chemical building block.

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Article Synopsis
  • Laccases are multicopper oxidases produced by white-rot fungi, with various isoforms useful in industrial applications, particularly in oxidizing phenolic compounds.
  • The study focuses on laccase 2 from Trametes polyzona (TP-Lac2), which operates optimally at 50 °C and can decolorize both phenolic and non-phenolic compounds under acidic conditions.
  • TP-Lac2 showed over 75% decolorization efficiency on multiple textile dyes when paired with mediators like acetosyringone and ABTS, highlighting its potential for eco-friendly wastewater treatment in the textile industry.
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Nowadays, the yeast is the platform of choice for demonstrating the proof of concept of the production of metabolites with a complex structure. However, introducing heterologous genes and rewiring the endogenous metabolism is still not standardized enough, affecting negatively the readiness-to-market of such metabolites. We developed the Easy Modular Integrative fuSion-ready Expression (Easy-MISE) toolkit, which is a novel combination of synthetic biology tools based on a single Golden Gate multiplasmid assembly meant to further ameliorate the rational predictability and flexibility of the process of yeast engineering.

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CRISPR-Cas9 technology is widely used for precise and specific editing of Saccharomyces cerevisiae genome to obtain marker-free engineered hosts. Targeted double-strand breaks are controlled by a guide RNA (gRNA), a chimeric RNA containing a structural segment for Cas9 binding and a 20-mer guide sequence that hybridises to the genomic DNA target. Introducing the 20-mer guide sequence into gRNA expression vectors often requires complex, time-consuming, and/or expensive cloning procedures.

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