Schiltz E, Schnackerz K D
Eur J Biochem. 1976 Dec;71(1):109-16. doi: 10.1111/j.1432-1033.1976.tb11095.x.
An improved procedure for large-scale production of crystalline D-serine dehydratase (EC 4.2.1.14) from Escherichia coli is described. The N-terminal sequence of the enzyme (Mr 45500) was determined in a solid-phase sequencer as Met-Glu-Asn-Ala-Lys-Met-Asn-Ser-Leu-Ile-Ala-Gln-Tyr-Pro-Leu-Val-Lys-Asp-Leu-Val-Ala-LEU-Lys. Four of the first five N-terminal residues are homologeous with tryptophanase, another pyridoxal-phosphate (P-Pxy) enzyme that catalyzes alpha,beta-elimination reactions. After borohydride reduction and tryptic digestion of the enzyme, a peptide was isolated showing the sequence Lys-Asp-Ser-His-Leu-Pro-Ile-Ser-Gly-Ser-Ile-Lys(P-Pxy)-Ala-Arg. No clear homology of this portion of the enzyme with tryptophanase or another pyridoxal-phosphate enzyme was observed.
本文描述了一种从大肠杆菌大规模生产结晶D-丝氨酸脱水酶(EC 4.2.1.14)的改进方法。在固相测序仪中测定了该酶(Mr 45500)的N端序列为Met-Glu-Asn-Ala-Lys-Met-Asn-Ser-Leu-Ile-Ala-Gln-Tyr-Pro-Leu-Val-Lys-Asp-Leu-Val-Ala-LEU-Lys。前五个N端残基中的四个与色氨酸酶同源,色氨酸酶是另一种催化α,β-消除反应的磷酸吡哆醛(P-Pxy)酶。对该酶进行硼氢化还原和胰蛋白酶消化后,分离出一个肽段,其序列为Lys-Asp-Ser-His-Leu-Pro-Ile-Ser-Gly-Ser-Ile-Lys(P-Pxy)-Ala-Arg。未观察到该酶的这一部分与色氨酸酶或其他磷酸吡哆醛酶有明显的同源性。