Difference between revisions of "Part:BBa K3699001"
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=='''Introduction'''== | =='''Introduction'''== | ||
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<figure><img src="https://static.igem.org/mediawiki/2014/0/05/Peking2014jyj_2.png"/><figcaption><b>Figure 1. First step of biodegradation of MC-LR.</b> MlrA mediates breaking peptide bond between Adda and Arg, which leads to significant decrease of toxicity.<sup>[1]</sup></figcaption></figure> | <figure><img src="https://static.igem.org/mediawiki/2014/0/05/Peking2014jyj_2.png"/><figcaption><b>Figure 1. First step of biodegradation of MC-LR.</b> MlrA mediates breaking peptide bond between Adda and Arg, which leads to significant decrease of toxicity.<sup>[1]</sup></figcaption></figure> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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<p>[1] Li J , Li R , Li J . Current research scenario for microcystins biodegradation - A review on fundamental knowledge, application prospects and challenges[J]. <i>ence of the Total Environment</i>, 2017, 595(OCT.1):615.</p> | <p>[1] Li J , Li R , Li J . Current research scenario for microcystins biodegradation - A review on fundamental knowledge, application prospects and challenges[J]. <i>ence of the Total Environment</i>, 2017, 595(OCT.1):615.</p> | ||
<p>[2] Gehringer M M , Milne P , Lucietto F , et al. Comparison of the structure of key variants of microcystin to vasopressin[J]. <i>Environmental Toxicology & Pharmacology</i>, 2005, 19(2):297-303.</p> | <p>[2] Gehringer M M , Milne P , Lucietto F , et al. Comparison of the structure of key variants of microcystin to vasopressin[J]. <i>Environmental Toxicology & Pharmacology</i>, 2005, 19(2):297-303.</p> | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
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Revision as of 01:31, 23 October 2020
MlrA from Novosphingobium sp. THN1
Introduction
This part is microcystin enzyme (MlrA) from Novosphingobium sp. THN1.
MlrA is an enzyme that degrades cyanobacterial toxins, especially microcystin-LR (MC-LR).
By comparing the ability of Sphingomonas sp. ACM-3962, Novosphingobium sp. THN1 and other bacteria’s data, we found Novosphingobium sp. THN1 shows a stronger activity. So we characterize it.
To promote enzyme expression, we replaced the commonly used strong promoter J23110 with the stronger J23119 in its family. This part successfully expressed MlrA enzyme and showed activity on degrading MC-LR.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]