Solution Structure and Conformational Flexibility of a Polyketide Synthase Module

• Published in: JACS Au Vol. 1; no. 12; pp. 2162 - 2171
• Main Authors: Klaus, Maja, Rossini, Emanuele, Linden, Andreas, Paithankar, Karthik S, Zeug, Matthias, Ignatova, Zoya, Urlaub, Henning, Khosla, Chaitan, Köfinger, Jürgen, Hummer, Gerhard, Grininger, Martin
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 27.12.2021
• ISSN: 2691-3704; 2691-3704
• DOI: 10.1021/jacsau.1c00043

Polyketide synthases (PKSs) are versatile C-C bond-forming enzymes that are broadly distributed in bacteria and fungi. The polyketide compound family includes many clinically useful drugs such as the antibiotic erythromycin, the antineoplastic epothilone, and the cholesterol-lowering lovastatin. Harnessing PKSs for custom compound synthesis remains an open challenge, largely because of the lack of knowledge about key structural properties. Particularly, the domains-well characterized on their own-are poorly understood in their arrangement, conformational dynamics, and interplay in the intricate quaternary structure of modular PKSs. Here, we characterize module 2 from the 6-deoxyerythronolide B synthase by small-angle X-ray scattering and cross-linking mass spectrometry with coarse-grained structural modeling. The results of this hybrid approach shed light on the solution structure of a cis-AT type PKS module as well as its inherent conformational dynamics. Supported by a directed evolution approach, we also find that acyl carrier protein (ACP)-mediated substrate shuttling appears to be steered by a nonspecific electrostatic interaction network.