|
Vol. 10, Issue 10, 1468-1484, October 2000
Biosynthesis of Isoprenoids via Mevalonate in Archaea: The Lost Pathway
Arian
Smit,1 and
Arcady
Mushegian2
1 Institute for Systems Biology,
Seattle, Washington 98195, USA; 2 Akkadix Corporation, La
Jolla, California 92037
Isoprenoid compounds are ubiquitous in living species and diverse in
biological function. Isoprenoid side chains of the membrane lipids are
biochemical markers distinguishing archaea from the rest of living
forms. The mevalonate pathway of isoprenoid biosynthesis has been
defined completely in yeast, while the alternative, deoxy-D-xylulose phosphate synthase pathway is found in many bacteria. In archaea, some
enzymes of the mevalonate pathway are found, but the orthologs of three
yeast proteins, accounting for the route from phosphomevalonate to
geranyl pyrophosphate, are missing, as are the enzymes from the
alternative pathway. To understand the evolution of isoprenoid biosynthesis, as well as the mechanism of lipid biosynthesis in archaea, sequence motifs in the known enzymes of the two pathways of
isoprenoid biosynthesis were analyzed. New sequence relationships were
detected, including similarities between diphosphomevalonate decarboxylase and kinases of the galactokinase superfamily, between the
metazoan phosphomevalonate kinase and the nucleoside monophosphate kinase superfamily, and between isopentenyl pyrophosphate isomerases and MutT pyrophosphohydrolases. Based on these findings, orphan members
of the galactokinase, nucleoside monophosphate kinase, and
pyrophosphohydrolase families in archaeal genomes were evaluated as
candidate enzymes for the three missing steps. Alternative methods of
finding these missing links were explored, including physical linkage
of open reading frames and patterns of ortholog distribution in
different species. Combining these approaches resulted in the
generation of a short list of 13 candidate genes for the three missing
functions in archaea, whose participation in isoprenoid biosynthesis is
amenable to biochemical and genetic investigation.
2
Corresponding author.
1
These and some other gi numbers relate to the
resubmission of the proteins to the NR database as the cured SWISS-PROT
entries; sequential numbering of the entries does not imply their
linkage in the genome unless specifically indicated.
10:1468-1484 ©2000 by Cold Spring Harbor Laboratory Press ISSN 1088-9051/00 $5.00

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
L. L. GROCHOWSKI and R. H. WHITE
Promiscuous Anaerobes: New and Unconventional Metabolism in Methanogenic Archaea
Ann. N.Y. Acad. Sci.,
March 1, 2008;
1125(1):
190 - 214.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. G. Skophammer, J. A. Servin, C. W. Herbold, and J. A. Lake
Evidence for a Gram-positive, Eubacterial Root of the Tree of Life
Mol. Biol. Evol.,
August 1, 2007;
24(8):
1761 - 1768.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. L. Grochowski, H. Xu, and R. H. White
Methanocaldococcus jannaschii Uses a Modified Mevalonate Pathway for Biosynthesis of Isopentenyl Diphosphate
J. Bacteriol.,
May 1, 2006;
188(9):
3192 - 3198.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Eichler and M. W. W. Adams
Posttranslational Protein Modification in Archaea
Microbiol. Mol. Biol. Rev.,
September 1, 2005;
69(3):
393 - 425.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. J. Barkley, R. M. Cornish, and C. D. Poulter
Identification of an Archaeal Type II Isopentenyl Diphosphate Isomerase in Methanothermobacter thermautotrophicus
J. Bacteriol.,
March 15, 2004;
186(6):
1811 - 1817.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Gensheimer and A. Mushegian
Chalcone isomerase family and fold: No longer unique to plants
Protein Sci.,
February 1, 2004;
13(2):
540 - 544.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Liu and A. Mushegian
Three monophyletic superfamilies account for the majority of the known glycosyltransferases
Protein Sci.,
July 1, 2003;
12(7):
1418 - 1431.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Pilloff, K. Dabovic, M. J. Romanowski, J. B. Bonanno, M. Doherty, S. K. Burley, and T. S. Leyh
The Kinetic Mechanism of Phosphomevalonate Kinase
J. Biol. Chem.,
February 7, 2003;
278(7):
4510 - 4515.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. B. Bonanno, C. Edo, N. Eswar, U. Pieper, M. J. Romanowski, V. Ilyin, S. E. Gerchman, H. Kycia, F. W. Studier, A. Sali, et al.
Structural genomics of enzymes involved in sterol/isoprenoid biosynthesis
PNAS,
November 6, 2001;
98(23):
12896 - 12901.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|