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家兔溶菌酶缺乏症的遗传

Inheritance of lysozyme deficiency in rabbits.

作者信息

Prieur D J, Cámara V M

出版信息

J Hered. 1979 May-Jun;70(3):181-4. doi: 10.1093/oxfordjournals.jhered.a109230.

Abstract

The phenotypes of 273 offspring of 56 matings of various genotypes of lysozyme-deficient and normal New Zealand white rabbits were analyzed. It was determined that lysozyme deficiency of rabbits is inherited as an autosomal recessive with complete penetrance. The symbol ld is suggested for the gene for lysozyme deficiency. Further studies on the nature of the condition revealed that the lysozyme deficiency was not due to a lysozyme that was cold labile, or to a lysozyme that was so tightly bound it was unavailable for enzymatic assay, or to a lysozyme with a variant pH optimum. It was demonstrated, however, that the pH profile of the lysozyme remaining in the ld/ld rabbits was different from that found in normal rabbits.

摘要

对56对不同基因型的溶菌酶缺陷型和正常新西兰白兔交配产生的273只后代的表型进行了分析。结果确定,兔的溶菌酶缺乏症是作为一种完全显性的常染色体隐性性状遗传的。建议用符号ld表示溶菌酶缺乏基因。对该病症性质的进一步研究表明,溶菌酶缺乏并非由于不耐冷的溶菌酶、紧密结合而无法进行酶活性测定的溶菌酶或具有不同最适pH值的溶菌酶。然而,已证明ld/ld兔体内剩余的溶菌酶的pH曲线与正常兔不同。

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