Abstract

Introduction. Discovering novel enzymes is of interest in both applied and basic science. Microbial enzymes, which are incredibly diverse and easy to produce, are increasingly sought by diverse approaches. Literature. This review first distinguishes culture-based from culture-independent methods, detailing within each group the advantages and drawbacks of sequence- and function-based methods. It then discusses the main factors affecting the success of endeavors to identify novel enzymes through construction and functional screening of genomic or metagenomic libraries: the sampled environment, how DNA is extracted and processed, the vector used (plasmid, cosmid, fosmid, BAC, or shuttle vector), the host cell chosen from the available prokaryotic and eukaryotic ones and the main screening steps. Conclusions. Library construction and screening can be tricky and requires expertise. Combining different strategies, such as working with cultivable and non-cultivable organisms, using sequence- and function-based approaches, or performing multihost screenings, is probably the best way to identify novel and diverse enzymes from an environmental sample.

Highlights

  • Discovering novel enzymes is of interest in both applied and basic science

  • The biggest limitations of using yeasts in functional screening could be poor recognition of heterologous promoters, low transformation yields, and the multiple enzymatic activities displayed by yeasts

  • As it is impossible to cover all the existing screening tests developed to date, we show the most important steps in functional screening

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Summary

Introduction

Discovering novel enzymes is of interest in both applied and basic science. Microbial enzymes, which are incredibly diverse and easy to produce, are increasingly sought by diverse approaches. This review first distinguishes culture-based from culture-independent methods, detailing within each group the advantages and drawbacks of sequence- and function-based methods It discusses the main factors affecting the success of endeavors to identify novel enzymes through construction and functional screening of genomic or metagenomic libraries: the sampled environment, how DNA is extracted and processed, the vector used (plasmid, cosmid, fosmid, BAC, or shuttle vector), the host cell chosen from the available prokaryotic and eukaryotic ones and the main screening steps. Library construction and screening can be tricky and requires expertise Combining different strategies, such as working with cultivable and non-cultivable organisms, using sequence- and function-based approaches, or performing multihost screenings, is probably the best way to identify novel and diverse enzymes from an environmental sample.

INTRODUCTION
TRADITIONAL AND CURRENT TECHNIQUES
Culture-dependent or independent approaches
Sequence-based approaches
Function-based approaches
SAMPLED ENVIRONMENTS
DNA EXTRACTION AND PROCESSING
Prokaryotic hosts
Eukaryotic hosts
FUNCTIONAL SCREENING OF LIBRARIES
CONCLUSIONS
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