Literature DB >> 10063

Thermothrix thioparus gen. et sp. nov. a facultatively anaerobic facultative chemolithotroph living at neutral pH and high temperature.

D E Caldwell, S J Caldwell, J P Laycock.   

Abstract

Thermothrix thioparus gen. et ep. nov. occurs naturally in a New Mexico hot spring at a temperature of 74 degrees C, a pH of 7.0, and a HS- concentration of 1 mg/litre. The organism is gram-negative, non-motile, 0.5-1.0 X 3-20 mum, and forms cell chains up to 1 cm in length. The resulting filaments do not possess a sheath. Sulfur is deposited extracellularly. The organism was isolated using an autotrophic medium with HS- as the energy source and NO3- as the terminal electron acceptor. Anaerobically either NO2- or NO3- is required, NO2- is formed from NO3-, and no observable gas is evolved. Oxygen can also be used as the terminal electron acceptor, but growth is poor because of the decreased solubility of O2 at temperatures required for growth. Alternate energy sources used aerobically and anaerobically include hexose, HS-, SO3-, and S2O3=. The temperature optimum is 70-73 degrees C and growth occurs from 62 to 77 degrees C. The organism's thermal and physiological characteristics are compared to those of Bacillus stearothermophilus, Methanobacterium thermoautotrophicum, Sulfolobus acidocalderius, Thermus aquaticus, Thermus flavus, as well as Thiobacillus denitrificans, the latter being the only other facultatively anaerobic chemolithotroph which has been isolated and described.

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Year:  1976        PMID: 10063     DOI: 10.1139/m76-223

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  15 in total

1.  Influence of sulfide and temperature on species composition and community structure of hot spring microbial mats.

Authors:  S Skirnisdottir; G O Hreggvidsson; S Hjörleifsdottir; V T Marteinsson; S K Petursdottir; O Holst; J K Kristjansson
Journal:  Appl Environ Microbiol       Date:  2000-07       Impact factor: 4.792

2.  Morphological survey of microbial mats near deep-sea thermal vents.

Authors:  H W Jannasch; C O Wirsen
Journal:  Appl Environ Microbiol       Date:  1981-02       Impact factor: 4.792

3.  Distribution of Thermus spp. in Icelandic Hot Springs and a Thermal Gradient.

Authors:  J K Kristjansson; G A Alfredsson
Journal:  Appl Environ Microbiol       Date:  1983-06       Impact factor: 4.792

4.  Filament formation in Thermus species in the presence of some D-amino acids or glycine.

Authors:  P H Janssen; L E Parker; H W Morgan
Journal:  Antonie Van Leeuwenhoek       Date:  1991-04       Impact factor: 2.271

5.  Unusual microorganisms observed in New Zealand hot springs.

Authors:  B K Patel; H W Morgan; R M Daniel
Journal:  Microb Ecol       Date:  1986-06       Impact factor: 4.552

6.  Evaluation of a proposed surface colonization equation usingThermothrix thiopara as a model organism.

Authors:  D K Brannan; D E Caldwell
Journal:  Microb Ecol       Date:  1982-06       Impact factor: 4.552

7.  The response of gram-negative, thermophilic bacteria to oxygen.

Authors:  G J Macmichael
Journal:  Microb Ecol       Date:  1988-03       Impact factor: 4.552

8.  Bacterial zonation, photosynthesis, and spectral light distribution in hot spring microbial mats of Iceland.

Authors:  B B Jørgensen; D C Nelson
Journal:  Microb Ecol       Date:  1988-09       Impact factor: 4.552

9.  Growth Kinetics and Yield Coefficients of the Extreme Thermophile Thermothrix thiopara in Continuous Culture.

Authors:  D K Brannan; D E Caldwell
Journal:  Appl Environ Microbiol       Date:  1983-01       Impact factor: 4.792

10.  Uracil-DNA glycosylase of thermophilic Thermothrix thiopara.

Authors:  O K Kaboev; L A Luchkina; T I Kuziakina
Journal:  J Bacteriol       Date:  1985-10       Impact factor: 3.490

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