K KYEREMEH, Ghana - Development of Novel Therapeutics for Parasite Infections and Cancer by Multi-step Microbial Biodiscovery Processes and iChip
K KYEREMEH, Ghana - Development of Novel Therapeutics for Parasite Infections and Cancer by Multi-step Microbial Biodiscovery Processes and iChip
批准号:
MR/S00520X/1
负责人:
Marcel Jaspars
金额:
$91.08万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2018
资助国家:
英国
项目状态:
未结题
起止时间:
2018 至 --
中文摘要
该项目旨在开发撒哈拉以南非洲巨大的微生物生物多样性,以创建一个具有生物合成能力的微生物的大型图书馆和一条新的化学结构管道,这些结构可用于开发治疗感染、癌症和寄生虫病的药物,这些疾病主要是撒哈拉以南非洲的地方病。该项目将利用该小组实验室中成熟的不同生物检测方法来筛选撒哈拉以南微生物的微生物化学多样性。最重要的是,我们的团队成员以非常高的标准履行某些功能的能力已经得到证实,这些功能包括:从土壤、植物、鱼类、螃蟹和食肉软体动物中分离和纯化大量自由生活的微生物;确定由这些微生物产生的分子的化学图谱;分子的分离和表征;利用微生物全基因组序列进行生物合成基因簇、生物信息学、敲除和异源表达沉默基因,以生产新的代谢物。在这项研究中,对选择性和有效活性的要求非常重要,因此,低水平的新微生物化学结构必须能够在不影响正常人类细胞的情况下杀死寄生虫或细菌。我们将对项目中获得的所有分子的生物活性进行详细的评估,为发现新的抗癌药物提供可能性。我们将组装总共300个西非新微生物菌株,分离、表征并测定它们在正常实验室培养条件下表达的分子的抗生素、抗寄生虫和抗癌特性。最重要的是,我们将找到诱导这些微生物表达一些在正常实验室条件下不易产生的分子的方法,方法是在许多定制的培养基和培养条件下生长它们,与联合真菌共培养,以及存在像一氧化氮这样的化学信号来激活沉默的生物合成基因簇的转录。此外,我们将使用生物信息学来识别沉默的基因簇,这些基因簇编码有效的抗生素、抗寄生虫和抗癌分子,敲除并在易于生长的细菌中异源表达这些基因,使其能够大量生产化合物。该项目将建立在所获得的化学结构的基础上,以创造一系列与药物一样活性但具有不同和更多改进特征的衍生物和类似物。这将有助于识别具有强大活性、低毒性、能够安全地给药并准备好在动物模块中进行测试的“铅”分子。
英文摘要
This project seeks to exploit the huge microbial biodiversity of sub-Saharan Africa to create a large library of biosynthetically talented microbes and a pipeline of novel chemical structures that can be used for the development of drugs for infections, cancer and parasitic diseases that are largely endemic to sub-Saharan Africa. The project will take advantage of different well established bioassays in the laboratories of this team to screen the microbial chemical diversity of sub-Saharan microbes. What is most important, is the already well-established ability of members of our team to perform to a very high standard certain functions including: isolation and purification of a large number of free-living microbes from soils, plants, fishes, crabs and carnivorous molluscs; chemical profiling to determine molecules that are produced by these microbes; isolation and characterization of molecules; exploitation of whole microbial genome sequences for biosynthetic gene clusters, bioinformatics, knockout and heterologous expression of silent genes for the production of novel metabolites. The requirement of selective and potent activity is very important in this research and hence low levels of novel microbial chemical structures must be able to kill parasites or bacteria without having an effect on normal human cells. The biological activity profiles of all the molecules obtained in the project will be evaluated into detail giving the possibility for the discovery of new anticancer agents.We will assemble a total of 300 novel West African microbial strains, isolate, characterize and determine the antibiotic, antiparasitic and anticancer properties of the molecules they express under normal laboratory culture conditions. Most importantly, we will find ways to induce these microbes to express some of the molecules that are not easily produced under normal laboratory conditions by growing them in many customized media and culture conditions, co-culture with co-associating fungi, and presence of chemical cues like nitric oxide known to activate transcription of silent biosynthetic gene clusters. Furthermore, we will use bioinformatics to identify silent gene clusters that encode for potent antibiotic, antiparasitic and anticancer molecules, knockout and heterologously express these genes in easy-to-grow bacteria that allows the production of compounds in sufficient quantities. This project will build on the chemical structures obtained to create a series of derivatives and analogues that are equally active but have different and more improved characteristics as drugs. This will facilitate the identification of a "lead" molecule with potent activity, low toxicity, the ability to be administered safely and ready for testing in animal modules.
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DOI:
10.3390/m1070
发表时间:
2019-09-01
期刊:
MOLBANK
影响因子:
0.6
作者:
[Dofuor, Aboagye Kwarteng, Kwain, Samuel, Kyeremeh, Kwaku]
通讯作者:
Kyeremeh, Kwaku
DOI:
10.1007/s11270-018-3766-5
发表时间:
2018-03
期刊:
Water, Air, & Soil Pollution
影响因子:
--
作者:
[F. Celik;Mustafa Camas;K. Kyeremeh;Anil Sazak Camas]
通讯作者:
F. Celik;Mustafa Camas;K. Kyeremeh;Anil Sazak Camas
DOI:
10.3390/synbio2010002
发表时间:
2024-01
期刊:
SynBio
影响因子:
--
作者:
[Saad Alrashdi;Federica Casolari;K. Kyeremeh;Hai Deng]
通讯作者:
Saad Alrashdi;Federica Casolari;K. Kyeremeh;Hai Deng
DOI:
10.3390/m1754
发表时间:
2024-03-01
期刊:
MOLBANK
影响因子:
0.6
作者:
[Alabed,Aziz, Kyeremeh,Kwaku, Deng,Hai]
通讯作者:
Deng,Hai
DOI:
10.3390/molecules28010354
发表时间:
2023-01-01
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
作者:
[Alrashdi S, Casolari F, Alabed A, Kyeremeh K, Deng H]
通讯作者:
Deng H
HOTBIO - A Holistic Approach to Training a new Generation of Scientists in Marine Biodiscovery
-
批准号:EP/X029999/1
-
项目类别:Research Grant
-
资助金额:$33.8万
-
财政年份:2023
-
负责人:Marcel Jaspars
-
依托单位:
Analysis of biological small molecule mixtures using multiple modes of mass spectrometric fragmentation coupled with new bioinformatics workflows
-
批准号:BB/X019802/1
-
项目类别:Research Grant
-
资助金额:$103.23万
-
财政年份:2023
-
负责人:Marcel Jaspars
-
依托单位:
Industrial scale production of cyanobactin enzymes for fast and efficient cyclic peptide synthesis
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批准号:BB/M013669/1
-
项目类别:Research Grant
-
资助金额:$18.58万
-
财政年份:2015
-
负责人:Marcel Jaspars
-
依托单位:
Enhanced productivity and functionality of Modified Ribosomally Produced Peptides (M-RIPPs)
-
批准号:BB/M028526/1
-
项目类别:Research Grant
-
资助金额:$58.98万
-
财政年份:2015
-
负责人:Marcel Jaspars
-
依托单位:
13TSB_SynBio Enhanced discovery and scalable synthesis of therapeutic cyclic peptides
-
批准号:BB/L004429/1
-
项目类别:Research Grant
-
资助金额:$17.98万
-
财政年份:2013
-
负责人:Marcel Jaspars
-
依托单位:
Biosynthesis of five-membered heterocyclic rings
-
批准号:BB/K015176/1
-
项目类别:Research Grant
-
资助金额:$7.69万
-
财政年份:2013
-
负责人:Marcel Jaspars
-
依托单位:
Biosynthesis and exploitation of marine-derived post-translationally modified ribosomal peptides
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批准号:BB/D020360/1
-
项目类别:Fellowship
-
资助金额:$26.22万
-
财政年份:2006
-
负责人:Marcel Jaspars
-
依托单位:
海外基金