Metabolic Diversity and Ecophysiology

2019 ◽  
pp. 65-112
Author(s):  
Colin B. Munn
Keyword(s):  
2012 ◽  
Author(s):  
Shirley F. Nishino ◽  
Jim C. Spain ◽  
Sarah H. Craven ◽  
Johana Husserl ◽  
Zohre Kurt ◽  
...  

2021 ◽  
Vol 61 (2) ◽  
pp. 88-109
Author(s):  
Ardhra Vijayan ◽  
Rejish Kumar Vattiringal Jayadradhan ◽  
Devika Pillai ◽  
Preena Prasannan Geetha ◽  
Valsamma Joseph ◽  
...  
Keyword(s):  

2021 ◽  
Vol 97 (3) ◽  
Author(s):  
Constantinos Xenophontos ◽  
Martin Taubert ◽  
W Stanley Harpole ◽  
Kirsten Küsel

ABSTRACT Quantifying the relative contributions of microbial species to ecosystem functioning is challenging, because of the distinct mechanisms associated with microbial phylogenetic and metabolic diversity. We constructed bacterial communities with different diversity traits and employed exoenzyme activities (EEAs) and carbon acquisition potential (CAP) from substrates as proxies of bacterial functioning to test the independent effects of these two aspects of biodiversity. We expected that metabolic diversity, but not phylogenetic diversity would be associated with greater ecological function. Phylogenetically relatedness should intensify species interactions and coexistence, therefore amplifying the influence of metabolic diversity. We examined the effects of each diversity treatment using linear models, while controlling for the other, and found that phylogenetic diversity strongly influenced community functioning, positively and negatively. Metabolic diversity, however, exhibited negative or non-significant relationships with community functioning. When controlling for different substrates, EEAs increased along with phylogenetic diversity but decreased with metabolic diversity. The strength of diversity effects was related to substrate chemistry and the molecular mechanisms associated with each substrate's degradation. EEAs of phylogenetically similar groups were strongly affected by within-genus interactions. These results highlight the unique flexibility of microbial metabolic functions that must be considered in further ecological theory development.


Peptides ◽  
2006 ◽  
Vol 27 (9) ◽  
pp. 2090-2103 ◽  
Author(s):  
Martin Welker ◽  
Blahoslav Maršálek ◽  
Lenka Šejnohová ◽  
Hans von Döhren

2008 ◽  
Vol 66 (3) ◽  
pp. 496-504 ◽  
Author(s):  
Christophe Chassard ◽  
Karen P. Scott ◽  
Perrine Marquet ◽  
Jennifer C. Martin ◽  
Christophe Del'homme ◽  
...  

Author(s):  
Weilan Gomes da Paixão Melo ◽  
Tássio Brito de Oliveira ◽  
Silvio Lovato Arcuri ◽  
Paula Benevides de Morais ◽  
Fernando Carlos Pagnocca
Keyword(s):  

2016 ◽  
Vol 60 (4) ◽  
pp. 303-313 ◽  
Author(s):  
Juhyun Kim ◽  
Manuel Salvador ◽  
Elizabeth Saunders ◽  
Jaime González ◽  
Claudio Avignone-Rossa ◽  
...  

The chassis is the cellular host used as a recipient of engineered biological systems in synthetic biology. They are required to propagate the genetic information and to express the genes encoded in it. Despite being an essential element for the appropriate function of genetic circuits, the chassis is rarely considered in their design phase. Consequently, the circuits are transferred to model organisms commonly used in the laboratory, such as Escherichia coli, that may be suboptimal for a required function. In this review, we discuss some of the properties desirable in a versatile chassis and summarize some examples of alternative hosts for synthetic biology amenable for engineering. These properties include a suitable life style, a robust cell wall, good knowledge of its regulatory network as well as of the interplay of the host components with the exogenous circuits, and the possibility of developing whole-cell models and tuneable metabolic fluxes that could allow a better distribution of cellular resources (metabolites, ATP, nucleotides, amino acids, transcriptional and translational machinery). We highlight Pseudomonas putida, widely used in many different biotechnological applications as a prominent organism for synthetic biology due to its metabolic diversity, robustness and ease of manipulation.


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