Toward Synthetic Biology Strategies for Adipic Acid Production: An in Silico Tool for Combined Thermodynamics and Stoichiometric Analysis of Metabolic Networks

代谢通量分析 代谢工程 己二酸 代谢网络 焊剂(冶金) 代谢途径 生物信息学 合成生物学 生物化学 代谢物 酿酒酵母 化学 生物 新陈代谢 计算生物学 有机化学 酵母 基因
作者
Nils J. H. Averesch,Verónica Martínez,Lars K. Nielsen,Jens O. Krömer
出处
期刊:ACS Synthetic Biology [American Chemical Society]
卷期号:7 (2): 490-509 被引量:26
标识
DOI:10.1021/acssynbio.7b00304
摘要

Adipic acid, a nylon-6,6 precursor, has recently gained popularity in synthetic biology. Here, 16 different production routes to adipic acid were evaluated using a novel tool for network-embedded thermodynamic analysis of elementary flux modes. The tool distinguishes between thermodynamically feasible and infeasible modes under determined metabolite concentrations, allowing the thermodynamic feasibility of theoretical yields to be assessed. Further, patterns that always caused infeasible flux distributions were identified, which will aid the development of tailored strain design. A review of cellular efflux mechanisms revealed that significant accumulation of extracellular product is only possible if coupled with ATP hydrolysis. A stoichiometric analysis demonstrated that the maximum theoretical product carbon yield heavily depends on the metabolic route, ranging from 32 to 99% on glucose and/or palmitate in Escherichia coli and Saccharomyces cerevisiae metabolic models. Equally important, metabolite concentrations appeared to be thermodynamically restricted in several pathways. Consequently, the number of thermodynamically feasible flux distributions was reduced, in some cases even rendering whole pathways infeasible, highlighting the importance of pathway choice. Only routes based on the shikimate pathway were thermodynamically favorable over a large concentration and pH range. The low pH capability of S. cerevisiae shifted the thermodynamic equilibrium of some pathways toward product formation. One identified infeasible-pattern revealed that the reversibility of the mitochondrial malate dehydrogenase contradicted the current state of knowledge, which imposes a major restriction on the metabolism of S. cerevisiae. Finally, the evaluation of industrially relevant constraints revealed that two shikimate pathway-based routes in E. coli were the most robust.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
慕青应助是鑫鑫采纳,获得10
1秒前
2秒前
斯文的小旋风应助淇淇采纳,获得20
3秒前
ICBC完成签到 ,获得积分10
3秒前
望北发布了新的文献求助10
4秒前
wubobo完成签到,获得积分10
5秒前
双离子完成签到,获得积分10
5秒前
Leo发布了新的文献求助10
5秒前
5秒前
科研力力发布了新的文献求助10
6秒前
情怀应助四月77采纳,获得10
6秒前
双离子发布了新的文献求助10
7秒前
慕青应助文艺谷蓝采纳,获得10
8秒前
JamesPei应助Ivy采纳,获得10
9秒前
10秒前
洛莉塔发布了新的文献求助10
10秒前
Owen应助追寻夜安采纳,获得10
11秒前
11秒前
开花发布了新的文献求助10
12秒前
赘婿应助成就的安阳采纳,获得10
12秒前
CipherSage应助黑炭球采纳,获得10
13秒前
14秒前
14秒前
15秒前
15秒前
圈圈叉叉发布了新的文献求助10
15秒前
lsy发布了新的文献求助10
15秒前
Yh发布了新的文献求助10
16秒前
Leo完成签到,获得积分10
17秒前
东方天奇完成签到 ,获得积分10
17秒前
科研通AI2S应助高山我梦采纳,获得10
18秒前
洛莉塔完成签到,获得积分10
18秒前
20秒前
汉堡包应助科研通管家采纳,获得10
21秒前
无花果应助科研通管家采纳,获得10
21秒前
酷波er应助科研通管家采纳,获得10
21秒前
搜集达人应助科研通管家采纳,获得10
21秒前
CodeCraft应助科研通管家采纳,获得10
21秒前
天天快乐应助科研通管家采纳,获得10
21秒前
高分求助中
Ophthalmic Equipment Market by Devices(surgical: vitreorentinal,IOLs,OVDs,contact lens,RGP lens,backflush,diagnostic&monitoring:OCT,actorefractor,keratometer,tonometer,ophthalmoscpe,OVD), End User,Buying Criteria-Global Forecast to2029 2000
A new approach to the extrapolation of accelerated life test data 1000
Cognitive Neuroscience: The Biology of the Mind 1000
Nucleophilic substitution in azasydnone-modified dinitroanisoles 500
不知道标题是什么 500
A Preliminary Study on Correlation Between Independent Components of Facial Thermal Images and Subjective Assessment of Chronic Stress 500
Technical Brochure TB 814: LPIT applications in HV gas insulated switchgear 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3962835
求助须知:如何正确求助?哪些是违规求助? 3508752
关于积分的说明 11142844
捐赠科研通 3241587
什么是DOI,文献DOI怎么找? 1791624
邀请新用户注册赠送积分活动 872998
科研通“疑难数据库(出版商)”最低求助积分说明 803540