Abstract

BackgroundThe development of transcriptomic tools has allowed exhaustive description of stress responses. These responses always superimpose a general response associated to growth rate decrease and a specific one corresponding to the stress. The exclusive growth rate response can be achieved through chemostat cultivation, enabling all parameters to remain constant except the growth rate.ResultsWe analysed metabolic and transcriptomic responses of Lactococcus lactis in continuous cultures at different growth rates ranging from 0.09 to 0.47 h-1. Growth rate was conditioned by isoleucine supply. Although carbon metabolism was constant and homolactic, a widespread transcriptomic response involving 30% of the genome was observed. The expression of genes encoding physiological functions associated with biogenesis increased with growth rate (transcription, translation, fatty acid and phospholipids metabolism). Many phages, prophages and transposon related genes were down regulated as growth rate increased. The growth rate response was compared to carbon and amino-acid starvation transcriptomic responses, revealing constant and significant involvement of growth rate regulations in these two stressful conditions (overlap 27%).Two regulators potentially involved in the growth rate regulations, llrE and yabB, have been identified. Moreover it was established that genes positively regulated by growth rate are preferentially located in the vicinity of replication origin while those negatively regulated are mainly encountered at the opposite, thus indicating the relationship between genes expression and their location on chromosome. Although stringent response mechanism is considered as the one governing growth deceleration in bacteria, the rigorous comparison of the two transcriptomic responses clearly indicated the mechanisms are distinct.ConclusionThis work of integrative biology was performed at the global level using transcriptomic analysis obtained in various growth conditions. It raised the importance of growth rate regulations in bacteria but also participated to the elucidation of the involved mechanism. Though the mechanism controlling growth rate is not yet fully understood in L. lactis, one expected regulatory mechanism has been ruled out, two potential regulators have been pointed out and the involvement of gene location on the chromosome has also been found to be involved in the expression regulation of these growth related genes.

Highlights

  • The development of transcriptomic tools has allowed exhaustive description of stress responses

  • Growth rate influence is major in bacteria and Egli and co-workers [11] demonstrated in chemostat culture that the sensitivity of Escherichia coli to stress was dependent on the specific growth rate

  • Growth rate response Culture parameters The growth rate of Lactococcus lactis was 5 fold increased in a chemostat culture from 0.09 to 0.47 h-1 which corresponds to a decrease of the generation time from 7.7 to 1.5 h

Read more

Summary

Introduction

The development of transcriptomic tools has allowed exhaustive description of stress responses These responses always superimpose a general response associated to growth rate decrease and a specific one corresponding to the stress. Mostly using transcriptomic approach, have exhaustively described the responses to various stresses in different bacteria [1,2,3,4] These studies performed in batch cultures do not allow the growth rate response to be described because influences of the specific stress and the growth rate are superimposed. The exclusive cellular response associated to growth rate changes can be achieved through chemostat cultivation This fermentation mode enables the growth rate to be changed by the dilution rate monitoring without modifying environmental or nutritional parameters [5]. A complete analysis combining chemostat cultivation and transcriptomic approach to clearly study the growth rate influence at the global level has never been performed in bacteria

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call