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从第勒尼安海中部东部海域采集的蟹壳样本中分离出的巴氏芽孢杆菌菌株(BM17)产生几丁质酶。

Production of chitinolytic enzymes by a strain (BM17) of Paenibacillus pabuli isolated from crab shells samples collected in the east sector of central Tyrrhenian Sea.

作者信息

Juarez-Jimenez Belen, Rodelas Belen, Martinez-Toledo M Victoria, Gonzalez-Lopez Jesus, Crognale Silvia, Gallo Anna M, Pesciaroli Chiara, Fenice Massimiliano

机构信息

Istituto del Agua, University of Granada, Granada, Spain.

出版信息

Int J Biol Macromol. 2008 Jul 1;43(1):27-31. doi: 10.1016/j.ijbiomac.2007.10.022. Epub 2007 Nov 4.

Abstract

Nineteen bacterial isolates were grown in shaken cultures in media containing chitin as carbon source and different additional nitrogen sources such as yeast nitrogen base (YNB), yeast extract (YE), corn steep liquor (CSL) and ammonium sulfate. Strain BM17 showed the highest activity (200 U/l) in medium containing Chitin (1%) and YNB (0.5%). Molecular analysis of the 16S rRNA gene showed that strain BM17 belongs to the species Paenibacillus pabuli (99.72% homology). The enzyme activity started after 12-24 h; exponential enzyme production was recorded from the 24th h and lasted till the 96th h of incubation when activity peaked to decrease thereafter. Medium optimisation was carried out by Response Surface Methodology (RSM) considering the effects of chitin, corn steep liquor and yeast extract. BM17 chitinolytic activity was induced by chitin but the increase of its concentration did not have significant effects on the enzyme activity. By contrast, the nitrogen source, particularly YE, strongly affected the enzyme production.

摘要

将19株细菌分离株在含有几丁质作为碳源以及不同额外氮源(如酵母氮碱(YNB)、酵母提取物(YE)、玉米浆(CSL)和硫酸铵)的培养基中进行摇瓶培养。菌株BM17在含有1%几丁质和0.5%YNB的培养基中表现出最高活性(200 U/l)。对16S rRNA基因的分子分析表明,菌株BM17属于巴氏芽孢杆菌(同源性为99.72%)。酶活性在12 - 24小时后开始;从第24小时开始记录到酶的指数生产阶段,持续到培养的第96小时,此时活性达到峰值,此后开始下降。考虑到几丁质、玉米浆和酵母提取物的影响,采用响应面法(RSM)进行培养基优化。几丁质可诱导BM17的几丁质酶活性,但其浓度增加对酶活性没有显著影响。相比之下,氮源,特别是YE,对酶的产生有强烈影响。

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