Abstract

Improving the health beneficial fatty acid content of meat and milk is a major challenge requiring an increased understanding of rumen lipid metabolism. In this study, we isolated and characterized rumen bacterial lipases/esterases using functional metagenomics. Metagenomic libraries were constructed from DNA extracted from strained rumen fluid (SRF), solid-attached bacteria (SAB) and liquid-associated rumen bacteria (LAB), ligated into a fosmid vector and subsequently transformed into an Escherichia coli host. Fosmid libraries consisted of 7,744; 8,448; and 7,680 clones with an average insert size of 30 to 35 kbp for SRF, SAB and LAB, respectively. Transformants were screened on spirit blue agar plates containing tributyrin for lipase/esterase activity. Five SAB and four LAB clones exhibited lipolytic activity, and no positive clones were found in the SRF library. Fosmids from positive clones were pyrosequenced and twelve putative lipase/esterase genes and two phospholipase genes retrieved. Although the derived proteins clustered into diverse esterase and lipase families, a degree of novelty was seen, with homology ranging from 40 to 78 % following BlastP searches. Isolated lipases/esterases exhibited activity against mostly short- to medium-chain substrates across a range of temperatures and pH. The function of these novel enzymes recovered in ruminal metabolism needs further investigation, alongside their potential industrial uses.Electronic supplementary materialThe online version of this article (doi:10.1007/s00253-014-6355-6) contains supplementary material, which is available to authorized users.

Highlights

  • Rumen lipid metabolism plays a significant role in regulating the overall lipid composition of microbial cells and of meat and milk produced by ruminants (Harfoot and Hazlewood 1997; Scollan et al 2006; Lourenço et al 2010; Shingfield et al 2013)

  • liquid-associated rumen bacteria (LAB) were obtained by performing the low-speed and high-speed centrifugal steps as described on the liquid fraction obtained after initial hand squeezing of the retrieved rumen sample

  • The metagenomic libraries consisted of a total of 23,872 clones: 7,744 from strained rumen fluid (SRF), 8,448 from solid-attached bacteria (SAB) and 7,680 from LAB, with a range of insert sizes of 30–35 kbp

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Summary

Introduction

Rumen lipid metabolism plays a significant role in regulating the overall lipid composition of microbial cells and of meat and milk produced by ruminants (Harfoot and Hazlewood 1997; Scollan et al 2006; Lourenço et al 2010; Shingfield et al 2013). Dietary lipids enter the rumen either as triglycerides (neutral lipids) in concentrate-based feeds or as glycolipids or phospholipids (polar lipids) in forages (Harfoot and Hazlewood 1997; Bauman et al 2003). Like sulpholipids, are present as minor components in forage (

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