Can constraint network analysis guide the identification phase of KnowVolution? A case study on improved thermostability of an endo-β-glucanase

https://doi.org/10.1016/j.csbj.2020.12.034Get rights and content
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Abstract

Cellulases are industrially important enzymes, e.g., in the production of bioethanol, in pulp and paper industry, feedstock, and textile. Thermostability is often a prerequisite for high process stability and improving thermostability without affecting specific activities at lower temperatures is challenging and often time-consuming. Protein engineering strategies that combine experimental and computational are emerging in order to reduce experimental screening efforts and speed up enzyme engineering campaigns. Constraint Network Analysis (CNA) is a promising computational method that identifies beneficial positions in enzymes to improve thermostability. In this study, we compare CNA and directed evolution in the identification of beneficial positions in order to evaluate the potential of CNA in protein engineering campaigns (e.g., in the identification phase of KnowVolution). We engineered the industrially relevant endoglucanase EGLII from Penicillium verruculosum towards increased thermostability. From the CNA approach, six variants were obtained with an up to 2-fold improvement in thermostability. The overall experimental burden was reduced to 40% utilizing the CNA method in comparison to directed evolution. On a variant level, the success rate was similar for both strategies, with 0.27% and 0.18% improved variants in the epPCR and CNA-guided library, respectively. In essence, CNA is an effective method for identification of positions that improve thermostability.

Abbreviations

CNA
Constraint Network Analysis
PCR
polymerase chain reaction
HTS
high-throughput screening
EGLII
endoglucanase II
SSM
site-saturation mutagenesis
MTP
96-well microtiter plates
CMC
carboxymethyl cellulose
MD
molecular dynamics
AU
absorbance units

Keywords

KnowVolution
Protein engineering
Constraint network analysis
Thermostability
Cellulase
GH5 endoglucanase

Cited by (0)

1

Shared first authors.

2

ORCID: 0000-0001-8134-1445.

3

ORCID: 0000-0001-5498-0911.

4

ORCID: 0000-0003-0089-7156.

5

ORCID: 0000-0003-4026-701X.

6

ORCID: 0000-0001-8613-1447.