Literature DB >> 19128318

Diversity of hopanoids and squalene-hopene cyclases across a tropical land-sea gradient.

Ann Pearson1, William D Leavitt, James P Sáenz, Roger E Summons, Mandy C-M Tam, Hilary G Close.   

Abstract

Bacterial hopanoids are ubiquitous in Earth surface environments. They hold promise as environmental and ecological biomarkers, if the phylogeny and physiological drivers of hopanoid biosynthesis can be linked with the distribution of hopanoids observed across a breadth of samples. Here we survey the diversity of hopanoid cyclases from a land-sea gradient across the island of San Salvador, in the easternmost part of the Bahamas. The distribution of lipids was determined for the same sites, for the first time overlaying quantification of bacteriohopanepolyols with sqhC phylogeny. The results are similar to previous reports: environmental sqhCs average < 65% translated amino acid identity to their closest named relatives, and sequences from putative Proteobacteria dominate. Additionally, a new and apparently ubiquitous group of marine hopanoid producers is identified; it has no identifiable close relatives. The greatest diversity of hopanoid lipids occurs in soil, but hopanoids represent a minor fraction of total soil-derived lipids. Marine samples contain fewer identifiable hopanoids, but they are more abundant as a fraction of the total extractable lipids. In soil, the dominant compounds are 35-aminobacteriohopane-32,33,34-triol and adenosylhopane. In an upper estuarine sample, bacteriohopanetetrol and 32,35-anhydrobacteriohopanetetrol dominate; while in lower estuarine and open marine samples, the most abundant are bacteriohopanetetrol and bacteriohopaneribonolactone. Cyclitol ethers are trace components in the soil, absent in the estuary, and of moderate abundance in the open marine setting, suggesting a dominant marine source. Conversely, aminotriol and aminotetrol decrease in abundance or disappear completely from land to ocean, while 2-methyldiplopterol shows the opposite trend. Small quantities of 2-methylbacteriohopanepolyols are detectable in all samples. The overall hopanoid distributions may correlate to the major phylogenetic families of hopanoid producers or to the environments in which they are found.

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Year:  2008        PMID: 19128318     DOI: 10.1111/j.1462-2920.2008.01817.x

Source DB:  PubMed          Journal:  Environ Microbiol        ISSN: 1462-2912            Impact factor:   5.491


  12 in total

1.  Identification of a methylase required for 2-methylhopanoid production and implications for the interpretation of sedimentary hopanes.

Authors:  Paula V Welander; Maureen L Coleman; Alex L Sessions; Roger E Summons; Dianne K Newman
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-26       Impact factor: 11.205

2.  Distribution and Abundance of Hopanoid Producers in Low-Oxygen Environments of the Eastern Pacific Ocean.

Authors:  Jenan J Kharbush; Kanchi Kejriwal; Lihini I Aluwihare
Journal:  Microb Ecol       Date:  2015-09-16       Impact factor: 4.552

3.  Hopanoid production is required for low-pH tolerance, antimicrobial resistance, and motility in Burkholderia cenocepacia.

Authors:  Crystal L Schmerk; Mark A Bernards; Miguel A Valvano
Journal:  J Bacteriol       Date:  2011-09-30       Impact factor: 3.490

4.  Community genomic analysis of an extremely acidophilic sulfur-oxidizing biofilm.

Authors:  Daniel S Jones; Heidi L Albrecht; Katherine S Dawson; Irene Schaperdoth; Katherine H Freeman; Yundan Pi; Ann Pearson; Jennifer L Macalady
Journal:  ISME J       Date:  2011-06-30       Impact factor: 10.302

5.  Composite bacterial hopanoids and their microbial producers across oxygen gradients in the water column of the California Current.

Authors:  Jenan J Kharbush; Juan A Ugalde; Shane L Hogle; Eric E Allen; Lihini I Aluwihare
Journal:  Appl Environ Microbiol       Date:  2013-09-27       Impact factor: 4.792

Review 6.  Squalene-hopene cyclases.

Authors:  Gabriele Siedenburg; Dieter Jendrossek
Journal:  Appl Environ Microbiol       Date:  2011-04-29       Impact factor: 4.792

7.  Exploring the existence of lipid rafts in bacteria.

Authors:  Marc Bramkamp; Daniel Lopez
Journal:  Microbiol Mol Biol Rev       Date:  2015-03       Impact factor: 11.056

8.  Identification and characterization of Rhodopseudomonas palustris TIE-1 hopanoid biosynthesis mutants.

Authors:  P V Welander; D M Doughty; C-H Wu; S Mehay; R E Summons; D K Newman
Journal:  Geobiology       Date:  2012-01-04       Impact factor: 4.407

9.  Quantitative hopanoid analysis enables robust pattern detection and comparison between laboratories.

Authors:  C-H Wu; L Kong; M Bialecka-Fornal; S Park; A L Thompson; G Kulkarni; S J Conway; D K Newman
Journal:  Geobiology       Date:  2015-04-11       Impact factor: 4.407

10.  Diverse capacity for 2-methylhopanoid production correlates with a specific ecological niche.

Authors:  Jessica N Ricci; Maureen L Coleman; Paula V Welander; Alex L Sessions; Roger E Summons; John R Spear; Dianne K Newman
Journal:  ISME J       Date:  2013-10-24       Impact factor: 10.302

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