Bock A K, Glasemacher J, Schmidt R, Schönheit P
Institut für Pflanzenphysiologie und Mikrobiologie, Freie Universität Berlin, D-14195 Berlin, Germany.
J Bacteriol. 1999 Mar;181(6):1861-7. doi: 10.1128/JB.181.6.1861-1867.1999.
Phosphate acetyltransferase (PTA) and acetate kinase (AK) of the hyperthermophilic eubacterium Thermotoga maritima have been purified 1,500- and 250-fold, respectively, to apparent homogeneity. PTA had an apparent molecular mass of 170 kDa and was composed of one subunit with a molecular mass of 34 kDa, suggesting a homotetramer (alpha4) structure. The N-terminal amino acid sequence showed significant identity to that of phosphate butyryltransferases from Clostridium acetobutylicum rather than to those of known phosphate acetyltransferases. The kinetic constants of the reversible enzyme reaction (acetyl-CoA + Pi -->/<-- acetyl phosphate + CoA) were determined at the pH optimum of pH 6.5. The apparent Km values for acetyl-CoA, Pi, acetyl phosphate, and coenzyme A (CoA) were 23, 110, 24, and 30 microM, respectively; the apparent Vmax values (at 55 degrees C) were 260 U/mg (acetyl phosphate formation) and 570 U/mg (acetyl-CoA formation). In addition to acetyl-CoA (100%), the enzyme accepted propionyl-CoA (60%) and butyryl-CoA (30%). The enzyme had a temperature optimum at 90 degrees C and was not inactivated by heat upon incubation at 80 degrees C for more than 2 h. AK had an apparent molecular mass of 90 kDa and consisted of one 44-kDa subunit, indicating a homodimer (alpha2) structure. The N-terminal amino acid sequence showed significant similarity to those of all known acetate kinases from eubacteria as well that of the archaeon Methanosarcina thermophila. The kinetic constants of the reversible enzyme reaction (acetyl phosphate + ADP -->/<-- acetate + ATP) were determined at the pH optimum of pH 7.0. The apparent Km values for acetyl phosphate, ADP, acetate, and ATP were 0.44, 3, 40, and 0.7 mM, respectively; the apparent Vmax values (at 50 degrees C) were 2,600 U/mg (acetate formation) and 1,800 U/mg (acetyl phosphate formation). AK phosphorylated propionate (54%) in addition to acetate (100%) and used GTP (100%), ITP (163%), UTP (56%), and CTP (21%) as phosphoryl donors in addition to ATP (100%). Divalent cations were required for activity, with Mn2+ and Mg2+ being most effective. The enzyme had a temperature optimum at 90 degrees C and was stabilized against heat inactivation by salts. In the presence of (NH4)2SO4 (1 M), which was most effective, the enzyme did not lose activity upon incubation at 100 degrees C for 3 h. The temperature optimum at 90 degrees C and the high thermostability of both PTA and AK are in accordance with their physiological function under hyperthermophilic conditions.
嗜热栖热菌(Thermotoga maritima)的磷酸乙酰转移酶(PTA)和乙酸激酶(AK)已分别纯化了1500倍和250倍,达到了明显的均一性。PTA的表观分子量为170 kDa,由一个分子量为34 kDa的亚基组成,表明其为同四聚体(α4)结构。其N端氨基酸序列与丙酮丁醇梭菌(Clostridium acetobutylicum)的磷酸丁酰转移酶有显著的一致性,而与已知的磷酸乙酰转移酶的序列不同。在pH最适值为6.5时测定了该可逆酶反应(乙酰辅酶A + 磷酸根⇌乙酰磷酸 + 辅酶A)的动力学常数。乙酰辅酶A、磷酸根、乙酰磷酸和辅酶A(CoA)的表观Km值分别为23、110、24和30 μM;表观Vmax值(在55℃时)分别为260 U/mg(乙酰磷酸生成)和570 U/mg(乙酰辅酶A生成)。除了乙酰辅酶A(100%)外,该酶还能接受丙酰辅酶A(60%)和丁酰辅酶A(30%)。该酶的最适温度为90℃,在80℃孵育2小时以上不会因热而失活。AK的表观分子量为90 kDa,由一个44 kDa的亚基组成,表明其为同二聚体(α2)结构。其N端氨基酸序列与所有已知的真细菌乙酸激酶以及嗜热嗜甲烷菌(Methanosarcina thermophila)的乙酸激酶有显著的相似性。在pH最适值为7.0时测定了该可逆酶反应(乙酰磷酸 + 二磷酸腺苷⇌乙酸 + 三磷酸腺苷)的动力学常数。乙酰磷酸、二磷酸腺苷、乙酸和三磷酸腺苷的表观Km值分别为0.44、3、40和0.7 mM;表观Vmax值(在50℃时)分别为2600 U/mg(乙酸生成)和1800 U/mg(乙酰磷酸生成)。AK除了能磷酸化乙酸(100%)外,还能磷酸化丙酸(54%),并且除了三磷酸腺苷(100%)外,还能使用鸟苷三磷酸(100%)、肌苷三磷酸(163%)、尿苷三磷酸(56%)和胞苷三磷酸(21%)作为磷酰基供体。活性需要二价阳离子,其中锰离子和镁离子最为有效。该酶的最适温度为90℃,并且盐能使其稳定而防止热失活。在最有效的硫酸铵(1 M)存在下,该酶在100℃孵育3小时不会失活。90℃的最适温度以及PTA和AK的高热稳定性与其在嗜热条件下的生理功能相符。