Tsai Y H, Lai W F, Wu Y W, Johnson L R
Graduate Institute of Cell and Molecular Biology, Taipei Medical College, Taiwan.
FEBS Lett. 1998 Sep 18;435(2-3):251-6. doi: 10.1016/s0014-5793(98)01062-x.
Tissue-transglutaminase (t-TGase) is a family of calcium-dependent enzymes. A Ca2+-independent soluble enzyme, in addition to t-TGase, capable of incorporating polyamines into proteins was demonstrated in rat intestinal mucosa. The Ca2+-independent enzyme was stimulated 2- to 5-fold by Fe2+ and Co2+ ions but inhibited by Cu2+ and Zn2+ ions. The Ca2+-stimulated t-TGase activity was inhibited by divalent ions in the following order: Zn2+, Fe2+ >Co2+ > Cu2+. The opposite effects of EGTA, Fe2+ and Co2+ on these two enzyme activities indicate that they are two distinct classes of enzymes. Competition studies demonstrated differential preferences of the two enzymes for substrates. The Ca2+-dependent enzyme preferred putrescine, monodansylcadaverine > cadaverine, spermidine, spermine > 1,10-diaminodecane > triethylbutylamine. On the other hand, the Ca2+-independent enzyme preferred putrescine > cadaverine > spermine, I,10-diaminodecane > spermidine > monodansylcadaverine > triethylbutylamine. Further studies with divalent ions excluded the possible association of this novel Ca2+-independent enzyme with diamine oxidase. Finally, the Ca2+-independent enzyme had a higher affinity for putrescine (Km = 0.02 mM) than did Ca2+-dependent t-TGase (0.2 mM). As judged by gel filtration on HiPrep Sephacryl 200 column, the Ca2+-independent enzyme had a molecular weight of approximately 48 kDa, the intestinal Ca2+-dependent t-TGase was about 188 kDa while that of testicular t-TGase was about 96 kDa. In conclusion, the Ca2+-independent enzyme is stimulated by cobalt or ferric ions, and selectively incorporates aliphatic diamines or polyamines with symmetric amino groups. The observed Ca2+-independent enzyme activity is not related to diamine oxidase or its products. With a 10 times greater affinity for putrescine, the calcium-independent, 48-kDa intestinal enzyme may mediate polyamine function better than calcium dependent, 188-kDa intestinal tissue transglutaminase in the intestinal mucosa.
组织转谷氨酰胺酶(t-TGase)是一类钙依赖性酶。在大鼠肠黏膜中发现了一种不依赖Ca2+的可溶性酶,除t-TGase外,它能够将多胺掺入蛋白质中。这种不依赖Ca2+的酶受到Fe2+和Co2+离子的2至5倍刺激,但受到Cu2+和Zn2+离子的抑制。Ca2+刺激的t-TGase活性受到二价离子的抑制,抑制顺序如下:Zn2+、Fe2+>Co2+>Cu2+。EGTA、Fe2+和Co2+对这两种酶活性的相反作用表明它们是两类不同的酶。竞争研究表明这两种酶对底物有不同的偏好。依赖Ca2+的酶优先选择腐胺、单丹磺酰尸胺>尸胺、亚精胺、精胺>1,10-二氨基癸烷>三乙丁胺。另一方面,不依赖Ca2+的酶优先选择腐胺>尸胺>精胺、1,10-二氨基癸烷>亚精胺>单丹磺酰尸胺>三乙丁胺。用二价离子进行的进一步研究排除了这种新型不依赖Ca2+的酶与二胺氧化酶可能存在的关联。最后,不依赖Ca2+的酶对腐胺的亲和力(Km = 0.02 mM)高于依赖Ca2+的t-TGase(0.2 mM)。通过在HiPrep Sephacryl 200柱上进行凝胶过滤判断,不依赖Ca2+的酶分子量约为48 kDa,肠中依赖Ca2+的t-TGase约为188 kDa,而睾丸t-TGase约为96 kDa。总之,不依赖Ca2+的酶受到钴或铁离子的刺激,并选择性地掺入具有对称氨基的脂肪族二胺或多胺。观察到的不依赖Ca2+的酶活性与二胺氧化酶或其产物无关。这种分子量为48 kDa的不依赖钙的肠酶对腐胺的亲和力比依赖钙的、分子量为188 kDa的肠组织转谷氨酰胺酶高10倍,可能在肠黏膜中比后者更好地介导多胺功能。