工业微生物
工業微生物
공업미생물
INDUSTRIAL MICROBIOLOGY
2015年
2期
47-54
,共8页
范如意%牛丹丹%应喜娟%沈微%陈献忠
範如意%牛丹丹%應喜娟%瀋微%陳獻忠
범여의%우단단%응희연%침미%진헌충
中温α-淀粉酶%解淀粉芽孢杆菌%地衣芽孢杆菌%异源表达
中溫α-澱粉酶%解澱粉芽孢桿菌%地衣芽孢桿菌%異源錶達
중온α-정분매%해정분아포간균%지의아포간균%이원표체
medium-temperature α-amylase%Bacillus amyliquefaciens%Bacillus licheniformis%heterologous expression
提高中温α-淀粉酶生产菌株的发酵温度,对减少冷却水消耗降低生产成本有重要意义。本文利用基因删除技术删除了地衣芽孢杆菌CBBD302菌株α-淀粉酶的编码基因(amyL)获得突变株D402。将表达解淀粉芽孢杆菌中温α-淀粉酶基因BaA的重组质粒pHY-WZX-BaA转化D402,获得表达中温α-淀粉酶的重组地衣芽孢杆菌D402/pHY-WZX-BaA。摇瓶发酵实验显示,重组菌最适发酵温度为42℃,比原生产菌株提高8℃,最高产酶水平达到301 U/mL。30 L发酵罐发酵试验,78 h达到最高酶活531 U/mL。重组酶的最适作用温度为60℃,最适作用pH 6.5,在90℃保温20 min可以完全失活,保持了中温α-淀粉酶既能在淀粉糊化温度下保持稳定又便于灭酶的优良性能。
提高中溫α-澱粉酶生產菌株的髮酵溫度,對減少冷卻水消耗降低生產成本有重要意義。本文利用基因刪除技術刪除瞭地衣芽孢桿菌CBBD302菌株α-澱粉酶的編碼基因(amyL)穫得突變株D402。將錶達解澱粉芽孢桿菌中溫α-澱粉酶基因BaA的重組質粒pHY-WZX-BaA轉化D402,穫得錶達中溫α-澱粉酶的重組地衣芽孢桿菌D402/pHY-WZX-BaA。搖瓶髮酵實驗顯示,重組菌最適髮酵溫度為42℃,比原生產菌株提高8℃,最高產酶水平達到301 U/mL。30 L髮酵罐髮酵試驗,78 h達到最高酶活531 U/mL。重組酶的最適作用溫度為60℃,最適作用pH 6.5,在90℃保溫20 min可以完全失活,保持瞭中溫α-澱粉酶既能在澱粉糊化溫度下保持穩定又便于滅酶的優良性能。
제고중온α-정분매생산균주적발효온도,대감소냉각수소모강저생산성본유중요의의。본문이용기인산제기술산제료지의아포간균CBBD302균주α-정분매적편마기인(amyL)획득돌변주D402。장표체해정분아포간균중온α-정분매기인BaA적중조질립pHY-WZX-BaA전화D402,획득표체중온α-정분매적중조지의아포간균D402/pHY-WZX-BaA。요병발효실험현시,중조균최괄발효온도위42℃,비원생산균주제고8℃,최고산매수평체도301 U/mL。30 L발효관발효시험,78 h체도최고매활531 U/mL。중조매적최괄작용온도위60℃,최괄작용pH 6.5,재90℃보온20 min가이완전실활,보지료중온α-정분매기능재정분호화온도하보지은정우편우멸매적우량성능。
To increase the fermentation temperature of α-amylase is of great significance for decreasing cooling water consumption and cost of production. In this study,the gene amyL encoding the thermostableα-amylase of B. licheniformis CBBD302 was deleted by homologous recombination. The resulting mutant strain B. licheniformis D402 was then used as a host cell to overexpress BaA. Afterwards,the recombinant plasmid pHY-WZX-BaA harboring the gene encoding B. amyloliquefaciens α-amylase (BaA)was constructed and transformed to D402 strain. The recombinant D402/pHY-WZX-BaA strain was obtained and also used for fermentation experiments. Under shake-flask conditions,the optimal fermen-tation temperature of the recombinant D402/pHY-WZX-BaA strain was 42 ℃. By comparison,the original strain B. amyloliquefaciens M23 exhibited optimal performance at 34 ℃. Furthermore,301 U/mL was the highest amount of produced enzyme obtained under the shake-flask condition and 531 U/mL was the highest amount of produced enzyme obtained after 78 h of fermentation in a 30 L fermentor. The recombinant enzyme showed an optimal performance at 60 ℃and pH 6. 5. This enzyme could also be inactivated completely by incubating at 90 ℃ for 20 min. Similar to the original products,the recombinant enzyme could remain stable at starch gelatinization temperature and be inactivated conveniently.