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  1. National Taiwan Ocean University Research Hub

Identify Domains Involving Activities of Candida rugosa Lipases and Create Novel Lipases from LIP1 and LIP4 Generated by Using in Vitro Evolution

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基本資料

Project title
Identify Domains Involving Activities of Candida rugosa Lipases and Create Novel Lipases from LIP1 and LIP4 Generated by Using in Vitro Evolution
Code/計畫編號
NSC91-2313-B019-040
Translated Name/計畫中文名
鑑定Candida rugosa脂肪脢活性區域和使用in Vitro Evolution產生新酵素
 
Project Coordinator/計畫主持人
Shye-Jye Tang
Funding Organization/主管機關
National Science and Technology Council
 
Department/Unit
Department of Bioscience and Biotechnology
Website
https://www.grb.gov.tw/search/planDetail?id=759250
Year
2002
 
Start date/計畫起
01-08-2002
Expected Completion/計畫迄
01-07-2003
 
Bugetid/研究經費
970千元
 
ResearchField/研究領域
生物科學
 

Description

Abstract
Candida rugosa 所產生的五種菌体外脂肪?(LIP-1~LIP-5),皆為534 個胺基酸,且在序列上具有高度的相似性,但卻有不同的基質特異性,由此可知CRL的序列與結構及基質特異性的相關性可能是非常嚴謹的。因此可利用蛋白質工程,將LIP-4 的序列改變,研究序列與蛋白質結構及基質特異性、熱穩定性之間的關係。以基因重組的方式,?生13 組的新式脂肪?NL-A ~ NL-M,但在E. coli系統中,只有NL-L 有活性反應,而NL-B 及NL-J 卻會在酵母菌系統中,因有醣基化(glycosylation)修飾,而回復其活性,其中NL-JF 與NL-J 只有三個胺基酸不同,卻因此造成沒有活性,推測可能是NL-JF 蛋白質序列中的S436L 有較大的可能性。在熱穩定性(Thermostability)的分析上,NL-J 雖然不是非常穩定,但因NL-L 的熱穩定性高。而NL-J 雖與LIP-4 的胺基酸只有28 個不同,且有95%的相同度(identity),但NL-J 的脂肪?活性相較於LIP-4 卻有非常明顯的增強,相對於不同的受質約有增強為1~4 倍左右,對Tributyrin (C4:0)而言,NL-J 是LIP-4 的1.7 倍左右,Tricapryin (C8:0)是2.2 倍,Tristearin (C18:0)是2.1 倍左右,Triolein (C18:1)是3.3倍左右,對Olive oil 而言是4.2 倍。而在Esterase Activity 中雖然整体而言NL-J均較LIP-4 低,但卻比Commercial lipase 高,約有2 ~ 3 倍的活性增強。而在NL-B與NL-L 方面,雖然皆與LIP-4 只有20 個胺基酸不同,且皆有95%的相同度(identity),但在脂肪?及酯解?的相對活性卻也是迥然不同。 The yeast Candida rugosa produces five extracellular lipases (LIP-1 ~ LIP-5) which encode 534 amino acid, showing high homology in sequence but diversity in the substrate specificity. These observations demonstrate that substrate specificity of CRL may be relative to the various CRL sequences. Using homologous recombination produces thirteen chimeric new lipases NL-A ~ NL-M. Only NL-L shows activity in E. coli expression system. In addition, NL-B and NL-J show activity in Saccharomyces cerevisiae expression system, that modify these LIPs with glycosylation. As comparison of NL-J, NL-JF does not show enzyme activity and its sequence only has differences of three amino acids. Thermostability of NL-J is showed the more stable than the other CRL. The difference of NL-J with LIP-4 has twenty-eight amino acids, and they demonstrate identity of 95%. The lipase activity of NL-J is more active than LIP-4, showing increase about 1 ~ 4 fold. The lipase activity of NL-J is increased in the substrates of tributyrin (C4:0), tricapryin (C8:0), tristearin (C18:0), triolein (C18:1) and olive oil about 1.7, 2.2, 2.1, 3.3 and 4.2 fold, respectively. The esterase activity of NL-J is less active than LIP-4 but NL-J increases 2 ~ 3 fold than commercial lipase in the esterase activity. Both NL-B and NL-L only have twenty amino acids differently, and they show ninety-five percent identity. However, they are different in the substrate specificity of lipase and esterase.
 
Keyword(s)
皺褶假絲酵母
脂肪酵素
酯解酵素
活性
Candida rugosa
Lipase
Esterase
Activity
 
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