Characterization of mitochondrial electron-transfer in Leishmania mexicana

被引:17
作者
Bermúdez, R [1 ]
Dagger, F [1 ]
D'Aquino, JA [1 ]
Benaim, G [1 ]
Dawidowicz, K [1 ]
机构
[1] Cent Univ Venezuela, Fac Ciencias, Inst Expt Biol, Caracas, Venezuela
关键词
mitochondrial; electron-transfer inhibitors; difference spectra; respiratory control; Leishmania mexicana;
D O I
10.1016/S0166-6851(97)00131-X
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
Some general features of the respiratory chain and respiratory control were characterized in coupled mitochondrial preparations from Leishmania mexicana promastigotes. O-2 uptake was sensitive to the electron-transfer inhibitors rotenone, flavone, malonate, 4,4,4-trifluoro-1-(2-thienyl) 1.3 butanedione (TTFA), antimycin A, 2n-nonyl-4-hydroxyquinoline-N-oxide (HQNO), myxothiazol, cyanide and azide. A high concentration of rotenone (60 mu M) was required to inhibit O-2 uptake effectively. Difference spectra revealed the presence of cytochromes (a + a(3)), b and c. Respiratory control was stimulated 2-fold by ADP with different exogenous oxidizable substrates. Calculated ADP/O ratios were consistent with the notion that ascorbate/N,N,N',N'-tetramethylphenylenediamine (TMPD)-linked and FAD-linked respiration proceeds, respectively, with one third and two thirds of the ATP producing capacity of NADH-linked respiration. State 3 was suppressed by the ATP synthase inhibitors oligomycin and aurovertin and by the adenine nucleotide translocator inhibitors atractyloside and carboxy atractyloside. The protonophore carbonyl cyanide p-(trifluoromethoxy)phenylhydrazone (FCCP) provoked state 3u respiration. The mitochondrial preparation was capable of Ca2+ uptake and Ca2+ stimulated respiration. Data obtained suggests strongly that mitochondrial complexes I, II, III and IV are present in a major pathway of electron-transfer and that oxidative phosphorylation might proceed with high bioenergetic efficiency. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:43 / 54
页数:12
相关论文
共 51 条
[1]  
ACKRELL BA, 1997, ARCH BIOCHEM BIOPHYS, V182, P107
[2]   TERMINAL OXIDASES IN THE TRYPANOSOMATID TRYPANOSOMA-CRUZI [J].
AFFRANCHINO, JL ;
DETARLOVSKY, MNS ;
STOPPANI, AOM .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1986, 85 (02) :381-388
[3]   RESPIRATORY CONTROL IN MITOCHONDRIA FROM TRYPANOSOMA-CRUZI [J].
AFFRANCHINO, JL ;
DETARLOVSKY, MNS ;
STOPPANI, AOM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1985, 16 (03) :289-298
[4]   PELLICULAR MICROTUBULES IN FAMILY TRYPANOSOMATIDAE [J].
ANGELOPOULOS, E .
JOURNAL OF PROTOZOOLOGY, 1970, 17 (01) :39-+
[5]   OXIDATION OF NADH BY A ROTENONE AND ANTIMYCIN-SENSITIVE PATHWAY IN THE MITOCHONDRION OF PROCYCLIC TRYPANOSOMA-BRUCEI-BRUCEI [J].
BEATTIE, DS ;
OBUNGU, VH ;
KIAIRA, JK .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 64 (01) :87-94
[6]   CA-2+ TRANSPORT IN ISOLATED MITOCHONDRIAL VESICLES FROM LEISHMANIA-BRAZILIENSIS PROMASTIGOTES [J].
BENAIM, G ;
BERMUDEZ, R ;
URBINA, JA .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1990, 39 (01) :61-68
[7]   MITOCHONDRIAL DEVELOPMENT IN TRYPANOSOMA-BRUCEI-BRUCEI TRANSITIONAL BLOOD-STREAM FORMS [J].
BIENEN, EJ ;
SARIC, M ;
POLLAKIS, G ;
GRADY, RW ;
CLARKSON, AB .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1991, 45 (02) :185-192
[8]   QUANTITATIVE ULTRASTRUCTURAL INVESTIGATIONS OF MITOCHONDRIAL DEVELOPMENT IN LEISHMANIA-DONOVANI DURING TRANSFORMATION [J].
BRUN, R ;
KRASSNER, SM .
JOURNAL OF PROTOZOOLOGY, 1976, 23 (04) :493-497
[9]   TECHNIQUES FOR THE ASSAY OF THE RESPIRATORY ENZYMES [J].
CHANCE, B .
METHODS IN ENZYMOLOGY, 1957, 4 :273-329
[10]  
CHANCE B, 1956, ADV ENZYMOL REL S BI, V17, P65