Holcenberg J S, Ericsson L, Roberts J
Biochemistry. 1978 Feb 7;17(3):411-7. doi: 10.1021/bi00596a005.
Acinetobactor glutaminase-asparaginase was treated with [6-14C]diazo-5-oxonorleucine, reduced with sodium borohydride, and cleaved with cyanogen bromide. Radioactivity was present only in a 96-residue-N-terminal peptide which eluted as the second peptide peak on Sephadex G-50. Radioactivity was released with the threonine in position 12 during automatic sequencing of this peptide. The amino acid sequence of a 60-residue tn-terminal segment and a 16-residue C-terminal segment of this peptide was determined. Pseudomonas 7 A glutaminase-asparaginase was treated with [6-14C]diazo-5-oxonorleucine and reduced with sodium borohydride. Radioactivity was released with the threonine in residue 20 during automatic sequencing of the whole enzyme. Analysis of 26 N-terminal residues showed that an 8-residue segment containing the radioactive threonine was identical with that in Acinetobacter glutaminase-asparaginase and in Escherichia coli asparaginase. Additional identical residues were noted in the N-terminal regions of these enzymes.
用[6-¹⁴C]重氮-5-氧代正亮氨酸处理不动杆菌谷氨酰胺酶-天冬酰胺酶,用硼氢化钠还原,并用溴化氰裂解。放射性仅存在于一个96个残基的N端肽段中,该肽段在Sephadex G-50上作为第二个肽峰洗脱。在该肽段的自动测序过程中,放射性与第12位的苏氨酸一起释放。测定了该肽段60个残基的N端片段和16个残基的C端片段的氨基酸序列。用[6-¹⁴C]重氮-5-氧代正亮氨酸处理假单胞菌7A谷氨酰胺酶-天冬酰胺酶,并用硼氢化钠还原。在全酶的自动测序过程中,放射性与第20位的苏氨酸一起释放。对26个N端残基的分析表明,一个包含放射性苏氨酸的8个残基片段与不动杆菌谷氨酰胺酶-天冬酰胺酶和大肠杆菌天冬酰胺酶中的片段相同。在这些酶的N端区域还发现了其他相同的残基。