Lu Jun, Zheng Yujuan, Yamagishi Hiromi, Odaka Masafumi, Tsujimura Masanari, Maeda Mizuo, Endo Isao
The Institute of Physical and Chemical Research, Wako Shi, 351-0198 Saitama, Japan.
FEBS Lett. 2003 Oct 23;553(3):391-6. doi: 10.1016/s0014-5793(03)01070-6.
Nitrile hydratase (NHase) activator from Rhodococcus sp. N-771 is required for NHase functional expression. The motif 73CXCC76 in the NHase activator sequence was here revealed to be vital for its function by site-directed mutagenesis. All three substitutions of the cysteines by serines resulted in a much lower level of expression of active NHase. Furthermore, interaction between NHase activator and NHase was detected and the critical role of NHase activator was not exhibited in the cysteine oxidization process of NHase. These findings suggest NHase activator mainly participates in iron trafficking in NHase biogenesis as an iron type metallochaperone.
来自红球菌属N-771的腈水合酶(NHase)激活剂是NHase功能表达所必需的。通过定点诱变发现,NHase激活剂序列中的基序73CXCC76对其功能至关重要。将半胱氨酸全部替换为丝氨酸导致活性NHase的表达水平大幅降低。此外,检测到NHase激活剂与NHase之间的相互作用,并且NHase激活剂的关键作用在NHase的半胱氨酸氧化过程中未表现出来。这些发现表明,NHase激活剂主要作为一种铁型金属伴侣参与NHase生物合成中的铁转运。