Homocysteine Is Biosynthesized from Aspartate Semialdehyde and Hydrogen Sulfide in Methanogenic Archaea

被引:19
作者
Allen, Kylie D. [1 ]
Miller, Danielle V. [1 ]
Rauch, Benjamin J. [2 ]
Perona, John J. [2 ,3 ]
White, Robert H. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Biochem, Blacksburg, VA 24061 USA
[2] Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97239 USA
[3] Portland State Univ, Dept Chem, Portland, OR 97201 USA
基金
美国国家科学基金会;
关键词
METHANOCOCCUS-JANNASCHII; MECHANISM; REDUCTASE; SULFUR; PROTEINS; CYSTEINE; REVEALS; CLUSTER; COMPLEX; ENZYME;
D O I
10.1021/acs.biochem.5b00118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The biosynthetic route for homocysteine, intermediate in methionine biosynthesis; is unknown in some methanogenic archaea because homologues of the canonical required genes cannot be identified. Here we demonstrate that Methanocaldococcus jannaschii can biosynthesize homocysteine from aspartate semialdehyde and hydrogen sulfide. Additionally, we confirm the genes involved in this new pathway in Methanosarcina acetivorans. A possible series of reactions in which a thioaldehyde is formed and then reduced to a thiol are proposed. This represents a novel route for the biosynthesis of homocysteine and exemplifies unique aspects of Sulfur chemistry occurring in prebiotic environments and in early life forms.
引用
收藏
页码:3129 / 3132
页数:4
相关论文
共 21 条
[1]  
Bolt C. J., 1996, SCIENCE, V273, P1058
[2]   Reaction mechanism of glyoxalase I explored by an X-ray crystallographic analysis of the human enzyme in complex with a transition state analogue [J].
Cameron, AD ;
Ridderström, M ;
Olin, B ;
Kavarana, MJ ;
Creighton, DJ ;
Mannervik, B .
BIOCHEMISTRY, 1999, 38 (41) :13480-13490
[3]   Heterodisulfide reductase from Methanothermobacter marburgensis contains an active-site [4Fe-4S] cluster that is directly involved in mediating heterodisulfide reduction [J].
Duin, EC ;
Madadi-Kahkesh, S ;
Hedderich, R ;
Clay, MD ;
Johnson, MK .
FEBS LETTERS, 2002, 512 (1-3) :263-268
[4]   The genome of M-acetivorans reveals extensive metabolic and physiological diversity [J].
Galagan, JE ;
Nusbaum, C ;
Roy, A ;
Endrizzi, MG ;
Macdonald, P ;
FitzHugh, W ;
Calvo, S ;
Engels, R ;
Smirnov, S ;
Atnoor, D ;
Brown, A ;
Allen, N ;
Naylor, J ;
Stange-Thomann, N ;
DeArellano, K ;
Johnson, R ;
Linton, L ;
McEwan, P ;
McKernan, K ;
Talamas, J ;
Tirrell, A ;
Ye, WJ ;
Zimmer, A ;
Barber, RD ;
Cann, I ;
Graham, DE ;
Grahame, DA ;
Guss, AM ;
Hedderich, R ;
Ingram-Smith, C ;
Kuettner, HC ;
Krzycki, JA ;
Leigh, JA ;
Li, WX ;
Liu, JF ;
Mukhopadhyay, B ;
Reeve, JN ;
Smith, K ;
Springer, TA ;
Umayam, LA ;
White, O ;
White, RH ;
de Macario, EC ;
Ferry, JG ;
Jarrell, KF ;
Jing, H ;
Macario, AJL ;
Paulsen, I ;
Pritchett, M ;
Sowers, KR .
GENOME RESEARCH, 2002, 12 (04) :532-542
[5]  
Grochowski LL, 2010, COMPREHENSIVE NATURAL PRODUCTS II: CHEMISTRY AND BIOLOGY, VOL 7: COFACTORS, P711
[6]   Enzymatic activation of sulfur for incorporation into biomolecules in prokaryotes [J].
Kessler, Dorothea .
FEMS MICROBIOLOGY REVIEWS, 2006, 30 (06) :825-840
[7]   Molecular characterization of lantibiotic-synthesizing enzyme EpiD reveals a function for bacterial Dfp proteins in coenzyme A biosynthesis [J].
Kupke, T ;
Uebele, M ;
Schmid, D ;
Jung, G ;
Blaesse, M ;
Steinbacher, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :31838-31846
[8]   THIOL ADDITION TO CARBONYL GROUP . EQUILIBRIA AND KINETICS [J].
LIENHARD, GE ;
JENCKS, WP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (17) :3982-&
[9]   Cysteine Is Not the Sulfur Source for Iron-Sulfur Cluster and Methionine Biosynthesis in the Methanogenic Archaeon Methanococcus maripaludis [J].
Liu, Yuchen ;
Sieprawska-Lupa, Magdalena ;
Whitman, William B. ;
White, Robert H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (42) :31923-31929
[10]   Binding of S-Methyl-5′-Thioadenosine and S-Adenosyl-L-Methionine to Protein MJ0100 Triggers an Open-to-Closed Conformational Change in Its CBS Motif Pair [J].
Lucas, Maria ;
Antonio Encinar, Jose ;
Astigarraga Arribas, Egoitz ;
Oyenarte, Iker ;
Gomez Garcia, Inmaculada ;
Kortazar, Danel ;
Fernandez, Jose A. ;
Mato, Jose M. ;
Luz Martinez-Chantar, Maria ;
Alfonso Martinez-Cruz, Luis .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 396 (03) :800-820