Narang S, Seawright J A
Biochem Genet. 1983 Oct;21(9-10):885-93. doi: 10.1007/BF00483947.
beta-Hydroxy acid dehydrogenase (beta-Had-2) of Anopheles albimanus was assigned to chromosome 3. The apparent sequence of loci on chromosome 3 is hexokinase-1--22--stripe--28--beta-hydroxy acid dehydrogenase-2--4--aldehyde oxidase--2--esterase-8--4--esterase-4--?--phosphoglucomutase--?--esterase-6. beta-Hydroxy acid dehydrogenase is 25 and 30 map units from phosphoglucomutase and esterase-6, respectively. The one-band electromorph of beta-Had-2 in homozygotes and the three-band type in heterozygotes suggest that the enzyme is a dimer. A variety of electrophoretic techniques and spectrophotometric analysis were used to determine if the allozymes of beta-Had-2 can be differentiated on a basis other than mobility. No differences were detected among the allozymes on the basis of thermostability, urea denaturation, response to thiol reagents, chelating agents, or changes in coenzyme and substrate concentrations. No heterogeneity within allozymes separated by electrophoresis was detected by using thermostability tests.
白纹伊蚊的β-羟基酸脱氢酶(β-Had-2)被定位到3号染色体上。3号染色体上基因座的明显顺序是己糖激酶-1--22--条带--28--β-羟基酸脱氢酶-2--4--醛氧化酶--2--酯酶-8--4--酯酶-4--?--磷酸葡萄糖变位酶--?--酯酶-6。β-羟基酸脱氢酶分别与磷酸葡萄糖变位酶和酯酶-6相距25和30个图距单位。纯合子中β-Had-2的单带电变体和杂合子中的三带类型表明该酶是二聚体。使用了多种电泳技术和分光光度分析来确定β-Had-2的同工酶是否可以基于迁移率以外的其他依据进行区分。在热稳定性、尿素变性、对硫醇试剂、螯合剂的反应或辅酶和底物浓度变化方面,未检测到同工酶之间的差异。通过热稳定性测试,未检测到电泳分离的同工酶内部存在异质性。