The enzymes involved in synthesis and utilization of carbamylphosphate in the deep-sea tube worm Riftia pachyptila

2000 ◽  
Vol 136 (1) ◽  
pp. 115-127 ◽  
Author(s):  
V. Simon ◽  
C. Purcarea ◽  
K. Sun ◽  
J. Joseph ◽  
G. Frebourg ◽  
...  
Keyword(s):  
Deep Sea ◽  
mBio ◽  
2019 ◽  
Vol 10 (6) ◽  
Author(s):  
Tjorven Hinzke ◽  
Manuel Kleiner ◽  
Corinna Breusing ◽  
Horst Felbeck ◽  
Robert Häsler ◽  
...  

ABSTRACT The deep-sea tubeworm Riftia pachyptila lacks a digestive system but completely relies on bacterial endosymbionts for nutrition. Although the symbiont has been studied in detail on the molecular level, such analyses were unavailable for the animal host, because sequence information was lacking. To identify host-symbiont interaction mechanisms, we therefore sequenced the Riftia transcriptome, which served as a basis for comparative metaproteomic analyses of symbiont-containing versus symbiont-free tissues, both under energy-rich and energy-limited conditions. Our results suggest that metabolic interactions include nutrient allocation from symbiont to host by symbiont digestion and substrate transfer to the symbiont by abundant host proteins. We furthermore propose that Riftia maintains its symbiont by protecting the bacteria from oxidative damage while also exerting symbiont population control. Eukaryote-like symbiont proteins might facilitate intracellular symbiont persistence. Energy limitation apparently leads to reduced symbiont biomass and increased symbiont digestion. Our study provides unprecedented insights into host-microbe interactions that shape this highly efficient symbiosis. IMPORTANCE All animals are associated with microorganisms; hence, host-microbe interactions are of fundamental importance for life on earth. However, we know little about the molecular basis of these interactions. Therefore, we studied the deep-sea Riftia pachyptila symbiosis, a model association in which the tubeworm host is associated with only one phylotype of endosymbiotic bacteria and completely depends on this sulfur-oxidizing symbiont for nutrition. Using a metaproteomics approach, we identified both metabolic interaction processes, such as substrate transfer between the two partners, and interactions that serve to maintain the symbiotic balance, e.g., host efforts to control the symbiont population or symbiont strategies to modulate these host efforts. We suggest that these interactions are essential principles of mutualistic animal-microbe associations.


Glycobiology ◽  
1998 ◽  
Vol 8 (7) ◽  
pp. 663-673 ◽  
Author(s):  
F. Zal ◽  
B. Kuster ◽  
G. Brian N. ◽  
D. J. Harvey ◽  
F. H. Lallier
Keyword(s):  
Deep Sea ◽  

2017 ◽  
Vol 19 (4) ◽  
pp. 345-350 ◽  
Author(s):  
Helu Liu ◽  
Hui Wang ◽  
Shanya Cai ◽  
Haibin Zhang
Keyword(s):  
Deep Sea ◽  

2017 ◽  
Vol 39 (6) ◽  
pp. 22-25
Author(s):  
Shana K. Goffredi

Forty years ago, scientists discovered an animal at the bottom of the ocean that changed forever how we view life on this planet. Abundant, thriving animals were not expected in the deep sea, due to the very low levels of organic carbon that sink down from above. The giant tubeworm Riftia pachyptila pays little attention to this problem, having renounced its mouth and digestive system during the course of evolution. Instead, this animal relies on a partnership with internal bacteria that act as a built-in source of nourishment and, in exchange, Riftia performs unparalleled physiological feats.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Tjorven Hinzke ◽  
Manuel Kleiner ◽  
Mareike Meister ◽  
Rabea Schlüter ◽  
Christian Hentschker ◽  
...  

The hydrothermal vent tubeworm Riftia pachyptila hosts a single 16S rRNA phylotype of intracellular sulfur-oxidizing symbionts, which vary considerably in cell morphology and exhibit a remarkable degree of physiological diversity and redundancy, even in the same host. To elucidate whether multiple metabolic routes are employed in the same cells or rather in distinct symbiont subpopulations, we enriched symbionts according to cell size by density gradient centrifugation. Metaproteomic analysis, microscopy, and flow cytometry strongly suggest that Riftia symbiont cells of different sizes represent metabolically dissimilar stages of a physiological differentiation process: While small symbionts actively divide and may establish cellular symbiont-host interaction, large symbionts apparently do not divide, but still replicate DNA, leading to DNA endoreduplication. Moreover, in large symbionts, carbon fixation and biomass production seem to be metabolic priorities. We propose that this division of labor between smaller and larger symbionts benefits the productivity of the symbiosis as a whole.


2019 ◽  
Vol 86 (1) ◽  
Author(s):  
Jessica H. Mitchell ◽  
Juliana M. Leonard ◽  
Jennifer Delaney ◽  
Peter R. Girguis ◽  
Kathleen M. Scott

ABSTRACT Use of hydrogen gas (H2) as an electron donor is common among free-living chemolithotrophic microorganisms. Given the presence of this dissolved gas at deep-sea hydrothermal vents, it has been suggested that it may also be a major electron donor for the free-living and symbiotic chemolithoautotrophic bacteria that are the primary producers at these sites. Giant Riftia pachyptila siboglinid tubeworms and their symbiotic bacteria (“Candidatus Endoriftia persephone”) dominate many vents in the Eastern Pacific, and their use of sulfide as a major electron donor has been documented. Genes encoding hydrogenase are present in the “Ca. Endoriftia persephone” genome, and proteome data suggest that these genes are expressed. In this study, high-pressure respirometry of intact R. pachyptila and incubations of trophosome homogenate were used to determine whether this symbiotic association could also use H2 as a major electron donor. Measured rates of H2 uptake by intact R. pachyptila in high-pressure respirometers were similar to rates measured in the absence of tubeworms. Oxygen uptake rates in the presence of H2 were always markedly lower than those measured in the presence of sulfide, as was the incorporation of 13C-labeled dissolved inorganic carbon. Carbon fixation by trophosome homogenate was not stimulated by H2, nor was hydrogenase activity detectable in these samples. Though genes encoding [NiFe] group 1e and [NiFe] group 3b hydrogenases are present in the genome and transcribed, it does not appear that H2 is a major electron donor for this system, and it may instead play a role in intracellular redox homeostasis. IMPORTANCE Despite the presence of hydrogenase genes, transcripts, and proteins in the “Ca. Endoriftia persephone” genome, transcriptome, and proteome, it does not appear that R. pachyptila can use H2 as a major electron donor. For many uncultivable microorganisms, omic analyses are the basis for inferences about their activities in situ. However, as is apparent from the study reported here, there are dangers in extrapolating from omics data to function, and it is essential, whenever possible, to verify functions predicted from omics data with physiological and biochemical measurements.


1998 ◽  
Vol 180 (6) ◽  
pp. 1596-1599 ◽  
Author(s):  
Jonathan J. Robinson ◽  
Jeffrey L. Stein ◽  
Colleen M. Cavanaugh

ABSTRACT The bacterial symbiont of the hydrothermal vent tubeworm fixes carbon via the Calvin-Benson cycle and has been shown previously to express a form II ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO). The gene cbbM, which encodes this enzyme, has been cloned and sequenced. The gene has the highest identity with thecbbM gene from Rhodospirillum rubrum, and analysis of the inferred amino acid sequence reveals that all active-site residues are conserved. This is the first form II RubisCO cloned and sequenced from a chemoautotrophic symbiont and from a deep-sea organism.


2004 ◽  
Vol 207 (3) ◽  
pp. 177-182 ◽  
Author(s):  
B. Govenar ◽  
M. Freeman ◽  
D. C. Bergquist ◽  
G. A. Johnson ◽  
C. R. Fisher

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