首页> 外文期刊>The Journal of Experimental Biology >Evidence for membrane-bound carbonic anhydrase in the air bladder of bowfin (Amia calva), a primitive air-breathing fish
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Evidence for membrane-bound carbonic anhydrase in the air bladder of bowfin (Amia calva), a primitive air-breathing fish

机译:原始呼吸鱼类bow鱼(Amia calva)的气囊中膜结合的碳酸酐酶的证据

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摘要

The purpose of this study was to examine the subcellular distribution and isoenzyme characteristics of carbonic anhydrase from the gills and respiratory air bladder of bowfin Amia calva, a primitive air-breathing fish. Separation of subcellular fractions by differential centrifugation revealed that the vast majority of carbonic anhydrase from the gills of bowfin originated from the cytoplasmic fraction. Washing of the gill microsomal pellet also indicated that the carbonic anhydrase originally associated with this pellet was largely due to contamination from the cytoplasmic fraction. Experiments with carbonic anhydrase inhibitor, sulphanilamide, and the plasma carbonic anhydrase inhibitor from this species confirmed that the bowfin gill probably contains only one carbonic anhydrase isoenzyme which had properties resembling those of CA II. In contrast to the situation in the gills, a relatively large percentage (27 %) of the total air bladder carbonic anhydrase was associated with the microsomal fraction. Washing of the air bladder microsomal pellet removed little of the carbonic anhydrase activity, indicating that most of the carbonic anhydrase in the microsomal fraction was associated with the membranes Like the mammalian pulmonary CA IV isoenzyme, microsomal carbonic anhydrase from the bowfin air bladder was less sensitive to the bowfin plasma carbonic anhydrase inhibitor, sodium dodecylsulphate (SDS) and sulphanilamide than was cytoplasmic carbonic anhydrase from the air bladder, Microsomal carbonic anhydrase from the bowfin air bladder also resembled CA IV in that it appears to be anchored to the membrane via a phosphatidylinositol-glycan linkage which could be cleaved by phosphatidylinositol-specific phospholipase C, Taken together, these results suggest that a membrane-bound carbonic anhydrase isoenzyme resembling mammalian CA IV in terms of inhibition characteristics and membrane attachment is present in the air-breathing organ of one of the most primitive air-breathing vertebrates. [References: 47]
机译:这项研究的目的是检查原始的呼吸鱼类bow鱼Amia calva的g和呼吸气囊中的碳酸酐酶的亚细胞分布和同工酶特性。通过差速离心分离亚细胞级分表明,鲍芬fin中的绝大多数碳酸酐酶来源于细胞质级分。 micro微粒沉淀物的洗涤还表明,最初与该沉淀物相关的碳酸酐酶很大程度上是由于细胞质部分的污染。用该物种的碳酸酐酶抑制剂,磺胺和血浆碳酸酐酶抑制剂进行的实验证实,bow鳍g可能只含有一种碳酸酐酶同工酶,其性质类似于CA II。与the的情况相反,总气囊碳酸酐酶的相对较大百分比(27%)与微粒体部分有关。清洗气囊微粒体沉淀物几乎没有去除碳酸酐酶的活性,这表明微粒体级分中的大多数碳酸酐酶与膜有关。就像哺乳动物的肺CA IV同工酶一样,来自弓翅形气囊的微粒碳酸酐酶的敏感性较低。与弓形血浆碳酸酐酶抑制剂,十二烷基硫酸钠(SDS)和丁磺酰胺相比,弓形气囊的微粒体碳酸酐酶与CA IV相似,因为它似乎是通过磷脂酰肌醇锚定在膜上的这些结果表明,磷脂酰肌醇特定的磷脂酶C可以裂解-β-聚糖键,这些结果表明,在一个人的呼吸器官中,在抑制特性和膜附着方面,类似于哺乳动物CA IV的膜结合的碳酸酐酶同工酶存在。最原始的呼吸椎骨特斯[参考:47]

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