Molecular phylogenetic and biogeochemical studies of sulfate-reducing bacteria in the rhizosphere of Spartina alterniflora

Citation
Me. Hines et al., Molecular phylogenetic and biogeochemical studies of sulfate-reducing bacteria in the rhizosphere of Spartina alterniflora, APPL ENVIR, 65(5), 1999, pp. 2209-2216
Citations number
65
Categorie Soggetti
Biology,Microbiology
Journal title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
ISSN journal
00992240 → ACNP
Volume
65
Issue
5
Year of publication
1999
Pages
2209 - 2216
Database
ISI
SICI code
0099-2240(199905)65:5<2209:MPABSO>2.0.ZU;2-2
Abstract
The population composition and biogeochemistry of sulfate-reducing bacteria (SRB) in the rhizosphere of the marsh grass Spartina alterniflora was inve stigated over two growing seasons by molecular probing, enumerations of cul turable SRB, and measurements of SO42- reduction rates and geochemical para meters. SO42- reduction was rapid in marsh sediments with rates up to 3.5 m u mol ml(-1) day(-1). Rates increased greatly when plant growth began in Ap ril and decreased again when plants flowered in late July. Results with nuc leic acid probes revealed that SRB rRNA accounted for up to 43% of the rRNA from members of the domain Bacteria in marsh sediments, with the highest p ercentages occurring in bacteria physically associated with root surfaces. The relative abundance (RA) of SRB rRNA in whole-sediment samples compared to that of Bacteria rRNA did not vary greatly throughout the year, despite Targe temporal changes in SO42- reduction activity. However, the RA of root -associated SRB did increase from <10 to >30% when plants were actively gro wing. rRNA from members of the family Desulfobacteriaceae comprised the maj ority of the SRB rRNA at 3 to 34% of Bacteria rRNA, with Desulfobulbus spp. accounting for 1 to 16%. The RA of Desulfovibrio rRNA generally comprised from <1 to 3% of the Bacteria rRNA. The highest Desulfobacteriaceae RA in w hole sediments was 26% and was found in the deepest sediment samples (6 to 8 cm). Culturable SRB abundance, determined by most-probable-number analyse s, was high at >10(7) ml(-1). Ethanol utilizers were most abundant, followe d by acetate utilizers. The high numbers of culturable SRB and the high RA of SRB rRNA compared to that of Bacteria rRNA may be due to the release of SRB substrates in plant root exudates, creating a microbial food web that c ircumvents fermentation.