...
首页> 外文期刊>Protein Engineering >Mutations to alter Aspergillus awamori glucoamylase selectivity. III. Asn20 -> Cys/Ala27 -> Cys, Ala27 -> Pro, Ser30 -> Pro, Lys108 -> Arg, Lys108 -> Met, Gly137 -> Ala, 311-314 loop, Tyr312 -> Trp and Ser436 -> Pro
【24h】

Mutations to alter Aspergillus awamori glucoamylase selectivity. III. Asn20 -> Cys/Ala27 -> Cys, Ala27 -> Pro, Ser30 -> Pro, Lys108 -> Arg, Lys108 -> Met, Gly137 -> Ala, 311-314 loop, Tyr312 -> Trp and Ser436 -> Pro

机译:改变泡盛曲霉葡糖淀粉酶选择性的突变。三, Asn20-> Cys / Ala27-> Cys,Ala27-> Pro,Ser30-> Pro,Lys108-> Arg,Lys108-> Met,Gly137-> Ala,311-314 loop,Tyr312-> Trp和Ser436-> Pro

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Mutations Asn20-->Cys/Ala27-->Cys (SS), Ala27-->Pro, Ser30-->Pro, Lys108-->Arg, Gly137-->Ala, Tyr312-->Trp and Ser436-->Pro in Aspergillus awamori glucoamylase, along with a mutation inserting a seven-residue loop between Tyr311 and Gly314 (311-314 Loop), were made to increase glucose yield from maltodextrin hydrolysis, No active Lys108-->Met glucoamylase was found in the supernatant after being expressed from yeast. Lys108-->Arg, 311-314 Loop and Tyr312-->Trp glucoamylases have lower activities than wild-type glucoamylase; other GAs have the same or higher activities, SS and 311-314 Loop glucoamylases give one-quarter to two-thirds the relative rates of isomaltose formation from glucose compared with glucose formation from maltodextrins at 35, 45 and 55 degrees C, correlating with up to 2% higher peak glucose yields from 30% (w/v) maltodextrin hydrolysis, Conversely, Lys108-->Arg glucoamylase has relative isomaltose formation rates three times higher and glucose yields up to 4% lower than wild-type glucoamylase, Gly137-->Ala and Tyr312-->Trp glucoamylases also give high glucose yields at higher temperatures, Mutated glucoamylases that catalyze high rates of isomaltose formation give higher glucose yields from shorter than from longer maltodextrins, opposite to normal experience with more efficient glucoamylases. [References: 67]
机译:突变Asn20-> Cys / Ala27-> Cys(SS),Ala27-> Pro,Ser30-> Pro,Lys108-> Arg,Gly137-> Ala,Tyr312-> Trp和Ser436->制成了泡盛曲霉葡糖淀粉酶的Pro,以及在Tyr311和Gly314之间插入七个残基环的突变(311-314环),以增加麦芽糖糊精水解的葡萄糖产量,在上清液中未发现活性的Lys108-> Met葡糖淀粉酶从酵母中表达出来。 Lys108-> Arg,311-314 Loop和Tyr312-> Trp葡糖淀粉酶的活性低于野生型葡糖淀粉酶;其他GA具有相同或更高的活性,SS和311-314环葡糖淀粉酶相对于35、45和55摄氏度麦芽糖糊精形成葡萄糖的相对比率,由葡萄糖形成异麦芽糖的相对速率为四分之一至三分之二,与反之,Lys108-> Arg葡糖淀粉酶的相对异麦芽糖形成速率比野生型葡糖淀粉酶Gly137-高30%(w / v),使最高葡萄糖产量提高2%,相反,Lys108-> Arg葡糖淀粉酶的相对异麦芽糖形成速率高三倍,而葡萄糖产量却低4%。 -> Ala和Tyr312-> Trp葡糖淀粉酶在较高温度下也能提供较高的葡萄糖产量,催化异麦芽糖形成率较高的突变葡糖淀粉酶比较短的麦芽糊精产生的葡萄糖产率更高,这与正常情况下使用更高效的葡糖淀粉酶的情况相反。 [参考:67]

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号