Expression of a Hyperthermophilic Cellobiohydrolase in Transgenic <i>Nicotiana tabacum</i> by Protein Storage Vacuole Targeting

• Main Authors: Manuel Benedetti, Valeria Vecchi, Zeno Guardini, Luca Dall’Osto, Roberto Bassi
• Format: Article
• Language: English
• Published: MDPI AG 2020-12-01
• Series: Plants
• Subjects: hyperthermophilic cellobiohydrolase; plant cell wall; protein storage vacuole; transgenic <i>Nicotiana tabacum</i>; plant immunity; saccharification
• Online Access: https://www.mdpi.com/2223-7747/9/12/1799

Plant expression of microbial Cell Wall Degrading Enzymes (CWDEs) is a valuable strategy to produce industrial enzymes at affordable cost. Unfortunately, the constitutive expression of CWDEs may affect plant fitness to variable extents, including developmental alterations, sterility and even lethality. In order to explore novel strategies for expressing CWDEs in crops, the cellobiohydrolase CBM3GH5, from the hyperthermophilic bacterium <i>Caldicellulosiruptor saccharolyticus</i>, was constitutively expressed in <i>N. tabacum</i> by targeting the enzyme both to the apoplast and to the protein storage vacuole. The apoplast targeting failed to isolate plants expressing the recombinant enzyme despite a large number of transformants being screened. On the opposite side, the targeting of the cellobiohydrolase to the protein storage vacuole led to several transgenic lines expressing CBM3GH5, with an enzyme yield of up to 0.08 mg g DW⁻¹ (1.67 Units g DW⁻¹) in the mature leaf tissue. The analysis of CBM3GH5 activity revealed that the enzyme accumulated in different plant organs in a developmental-dependent manner, with the highest abundance in mature leaves and roots, followed by seeds, stems and leaf ribs. Notably, both leaves and stems from transgenic plants were characterized by an improved temperature-dependent saccharification profile.