NARA Discovery
Article Details
← Back to Search Results
Journal Article

Molecular genetic analysis of a dimethylsulfoniopropionate lyase that liberates the climate‐changing gas dimethylsulfide in several marine α‐proteobacteria and Rhodobacter sphaeroides

A. R. J. Curson; R. Rogers; J. D. Todd; C. A. Brearley; A. W. B. Johnston
Environmental Microbiology · Vol. 10, Issue 3 · pp. 757-767 · 2008

Abstract

Summary The α‐proteobacterium Sulfitobacter EE‐36 makes the gas dimethylsulfide (DMS) from dimethylsulfoniopropionate (DMSP), an abundant antistress molecule made by many marine phytoplankton. We screened a cosmid library of Sulfitobacter for clones that conferred to other bacteria the ability to make DMS. One gene, termed dddL , was sufficient for this phenotype when cloned in pET21a and introduced into Escherichia coli . Close DddL homologues exist in the marine α‐proteobacteria Fulvimarina , Loktanella Oceanicola and Stappia , all of which made DMS when grown on DMSP. There was also a dddL homologue in Rhodobacter sphaeroides strain 2.4.1, but not in strain ATCC 17025; significantly, the former, but not the latter, emits DMS when grown with DMSP. Escherichia coli containing the cloned, overexpressed dddL genes of R. sphaeroides 2.4.1 and Sulfitobacter could convert DMSP to acrylate plus DMS. This is the first identification of such a ‘DMSP lyase’. Thus, DMS can be made either by this DddL lyase or by a DMSP acyl CoA transferase, specified by dddD , a gene that we had identified in several other marine bacteria.

Bibliographic Information

JournalEnvironmental Microbiology
PublisherWiley
Publication Date2008-03-01
Publication Year2008
Volume10
Issue3
Pages757-767
Document TypeJournal Article
Print ISSN1462-2912
eISSN1462-2920
DOI10.1111/j.1462-2920.2007.01499.x
SubjectMicrobial Ecology

Access Information

NARA Access Coverage1999-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/14622920
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.