集美大学学报(自然科学版)
集美大學學報(自然科學版)
집미대학학보(자연과학판)
Journal of Jimei University(Natural Science)
2015年
5期
356-364
,共9页
郭小红%刘艳苓%姜泽东%李利君%朱艳冰%倪辉%蔡慧农
郭小紅%劉豔苓%薑澤東%李利君%硃豔冰%倪輝%蔡慧農
곽소홍%류염령%강택동%리리군%주염빙%예휘%채혜농
柚皮%柚苷酶%固态发酵%成本估算%比活力
柚皮%柚苷酶%固態髮酵%成本估算%比活力
유피%유감매%고태발효%성본고산%비활력
pomelo peel%naringinase%solid-state fermentation%cost estimation%specific activity
以棘孢曲霉为菌种, 以磷酸氢二铵为氮源固态发酵柚皮生产柚苷酶, 结果表明, 在以柚皮为碳源和磷酸氢二铵为氮源的发酵体系中, 添加疏松剂和豆饼粉对柚苷酶发酵没有显著影响, 而磷酸氢二铵添加量和水分质量分数对柚苷酶合成具有显著影响. 当无水柚皮粉中磷酸氢二铵和水分质量分数分别为324%和1700%时,有利于提高柚苷酶发酵活力. 在接种量为71%、 发酵温度为30℃的情况下发酵6 d, 柚苷酶比合成速率与棘孢曲霉的生长速率符合模型Y柚苷酶 = 62677 X -0. 0381 , 其中Y代表柚苷酶的比合成速率, X代表比生长速率. 用Davis法测得柚苷酶活力为9461 IU/g, 酶发酵的培养基成本 (5 × 10-5元/IU) 远远低于其他同类研究, 酶的纯度远高于用豆饼粉为氮源所获得的酶纯度.
以棘孢麯黴為菌種, 以燐痠氫二銨為氮源固態髮酵柚皮生產柚苷酶, 結果錶明, 在以柚皮為碳源和燐痠氫二銨為氮源的髮酵體繫中, 添加疏鬆劑和豆餅粉對柚苷酶髮酵沒有顯著影響, 而燐痠氫二銨添加量和水分質量分數對柚苷酶閤成具有顯著影響. 噹無水柚皮粉中燐痠氫二銨和水分質量分數分彆為324%和1700%時,有利于提高柚苷酶髮酵活力. 在接種量為71%、 髮酵溫度為30℃的情況下髮酵6 d, 柚苷酶比閤成速率與棘孢麯黴的生長速率符閤模型Y柚苷酶 = 62677 X -0. 0381 , 其中Y代錶柚苷酶的比閤成速率, X代錶比生長速率. 用Davis法測得柚苷酶活力為9461 IU/g, 酶髮酵的培養基成本 (5 × 10-5元/IU) 遠遠低于其他同類研究, 酶的純度遠高于用豆餅粉為氮源所穫得的酶純度.
이극포곡매위균충, 이린산경이안위담원고태발효유피생산유감매, 결과표명, 재이유피위탄원화린산경이안위담원적발효체계중, 첨가소송제화두병분대유감매발효몰유현저영향, 이린산경이안첨가량화수분질량분수대유감매합성구유현저영향. 당무수유피분중린산경이안화수분질량분수분별위324%화1700%시,유리우제고유감매발효활력. 재접충량위71%、 발효온도위30℃적정황하발효6 d, 유감매비합성속솔여극포곡매적생장속솔부합모형Y유감매 = 62677 X -0. 0381 , 기중Y대표유감매적비합성속솔, X대표비생장속솔. 용Davis법측득유감매활력위9461 IU/g, 매발효적배양기성본 (5 × 10-5원/IU) 원원저우기타동류연구, 매적순도원고우용두병분위담원소획득적매순도.
The naringinase production from Aspergillus aculeatus was investigated using ( NH4 ) 2 HPO4 as nitrogen source in pomelo peel fermentation. The results showed that naringinase activity did not significantly increase by adding loosening agents and soybean meal powder, while the content of diammonium hydrogen phosphate and water had significant influence on naringinase production. The composition of the optimal medi-um included anhydrous citrus peel powder, the percentage rates for other ingredients in anhydrous citrus peel powder were as follow: diammonium hydrogen phosphate, 324%; water, 1700%. By using the fermen-tation condition of inoculum size 71% and fermentation temperature 30 ℃, the naringinase fermentation was estimated to have a naringinase synthesis model Ynaringinase =62677 X-0. 0381 , where Y represented the en-zymatic specific synthetic rate and X was the specific growth rate. After fermentation for 6 days, naringinase activity attained 9461 IU/g by Davis method analysis, higher than most research before reported. In addi- tion, the medium cost was merely 5 × 10 -5 Yuan/IU naringinase, much lower than those previous studies. Furthermore, the enzyme extract revealed higher purity than that in our previous study.