TY - JOUR
T1 - Genome sequence of Thermofilum pendens reveals an exceptional loss of biosynthetic pathways without genome reduction
AU - Anderson, Iain
AU - Rodriguez, Jason
AU - Susanti, Dwi
AU - Porat, Iris
AU - Reich, Claudia
AU - Ulrich, Luke E.
AU - Elkins, James G.
AU - Mavromatis, Kostas
AU - Lykidis, Athanasios
AU - Kim, Edwin
AU - Thompson, Linda S.
AU - Nolan, Matt
AU - Land, Miriam
AU - Copeland, Alex
AU - Lapidus, Alla
AU - Lucas, Susan
AU - Detter, Chris
AU - Zhulin, Igor B.
AU - Olsen, Gary J.
AU - Whitman, William
AU - Mukhopadhyay, Biswarup
AU - Bristow, James
AU - Kyrpides, Nikos
PY - 2008/4
Y1 - 2008/4
N2 - We report the complete genome of Thermofilum pendens, a deeply branching, hyperthermophilic member of the order Thermoproteales in the archaeal kingdom Crenarchaeota. T. pendens is a sulfur-dependent, anaerobic heterotroph isolated from a solfatara in Iceland. It is an extracellular commensal, requiring an extract of Thermoproteus tenax for growth, and the genome sequence reveals that biosynthetic pathways for purines, most amino acids, and most cofactors are absent. In fact, T. pendens has fewer biosynthetic enzymes than obligate intracellular parasites, although it does not display other features that are common among obligate parasites and thus does not appear to be in the process of becoming a parasite. It appears that T. pendens has adapted to life in an environment rich in nutrients. T. pendens was known previously to utilize peptides as an energy source, but the genome revealed a substantial ability to grow on carbohydrates. T. pendens is the first crenarchaeote and only the second archaeon found to have a transporter of the phosphotransferase system. In addition to fermentation, T. pendens may obtain energy from sulfur reduction with hydrogen and formate as electron donors. It may also be capable of sulfur-independent growth on formate with formate hydrogen lyase. Additional novel features are the presence of a monomethylamine:corrinoid methyltransferase, the first time that this enzyme has been found outside the Methanosarcinales, and the presence of a presenilin-related protein. The predicted highly expressed proteins do not include proteins encoded by housekeeping genes and instead include ABC transporters for carbohydrates and peptides and clustered regularly interspaced short palindromic repeat-associated proteins.
AB - We report the complete genome of Thermofilum pendens, a deeply branching, hyperthermophilic member of the order Thermoproteales in the archaeal kingdom Crenarchaeota. T. pendens is a sulfur-dependent, anaerobic heterotroph isolated from a solfatara in Iceland. It is an extracellular commensal, requiring an extract of Thermoproteus tenax for growth, and the genome sequence reveals that biosynthetic pathways for purines, most amino acids, and most cofactors are absent. In fact, T. pendens has fewer biosynthetic enzymes than obligate intracellular parasites, although it does not display other features that are common among obligate parasites and thus does not appear to be in the process of becoming a parasite. It appears that T. pendens has adapted to life in an environment rich in nutrients. T. pendens was known previously to utilize peptides as an energy source, but the genome revealed a substantial ability to grow on carbohydrates. T. pendens is the first crenarchaeote and only the second archaeon found to have a transporter of the phosphotransferase system. In addition to fermentation, T. pendens may obtain energy from sulfur reduction with hydrogen and formate as electron donors. It may also be capable of sulfur-independent growth on formate with formate hydrogen lyase. Additional novel features are the presence of a monomethylamine:corrinoid methyltransferase, the first time that this enzyme has been found outside the Methanosarcinales, and the presence of a presenilin-related protein. The predicted highly expressed proteins do not include proteins encoded by housekeeping genes and instead include ABC transporters for carbohydrates and peptides and clustered regularly interspaced short palindromic repeat-associated proteins.
UR - http://www.scopus.com/inward/record.url?scp=41949089913&partnerID=8YFLogxK
U2 - 10.1128/JB.01949-07
DO - 10.1128/JB.01949-07
M3 - Article
C2 - 18263724
AN - SCOPUS:41949089913
SN - 0021-9193
VL - 190
SP - 2957
EP - 2965
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 8
ER -