growth yields
Recently Published Documents


TOTAL DOCUMENTS

157
(FIVE YEARS 14)

H-INDEX

34
(FIVE YEARS 2)

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Xiao-Lin Chu ◽  
Quan-Guo Zhang

Abstract Background Mutation accumulation (MA) has profound ecological and evolutionary consequences. One example is that accumulation of conditionally neutral mutations leads to fitness trade-offs among heterogenous habitats which cause population divergence. Here we suggest that temperature, which controls the rates of all biochemical and biophysical processes, should play a crucial role for determining mutational effects. Particularly, warmer temperatures may mitigate the effects of some, not all, deleterious mutations and cause stronger environmental dependence in MA effects. Results We experimentally tested the above hypothesis by measuring the growth performance of ten Escherichia coli genotypes on six carbon resources across ten temperatures, where the ten genotypes were derived from a single ancestral strain and accumulated spontaneous mutations. We analyzed resource dependence of MA consequences for growth yields. The MA genotypes typically showed reduced growth yields relative to the ancestral type; and the magnitude of reduction was smaller at intermediate temperatures. Stronger resource dependence in MA consequences for growth performance was observed at higher temperatures. Specifically, the MA genotypes were more likely to show impaired growth performance on all the six carbon resources when grown at lower temperatures; but suffered growth performance loss only on some, not all the six, carbon substrates at higher temperatures. Conclusions Higher temperatures increase the chance that MA causes conditionally neutral fitness effects while MA is more likely to cause fitness loss regardless of available resources at lower temperatures. This finding has implications for understanding how geographic patterns in population divergence may emerge, and how conservation practices, particularly protection of diverse microhabitats, may mitigate the impacts of global warming.


2020 ◽  
Vol 15 (5) ◽  
pp. 711-719
Author(s):  
Muhammad Ansar ◽  
Bahrudin ◽  
Saiful Darman ◽  
Paiman

This study aims to improve the growth, yield, and quality of LP-VoS bulbs by applying bokashi fertilizer from goat manure and regulating the duration of water supply with a sprinkler irrigation system. This research is a field that arranged in split-plot design. The main plot is the duration of irrigation water supply, consisting of three levels, 0.5; 1,0; and 1.5 hours. The subplot is giving organic fertilizer bokashi goat manure, which consists of two kinds, namely: without bokashi fertilizer and the addition of bokashi fertilizer 15 t.ha-1. Each treatment was repeated three times so that in total, there were 18 experimental plot units. The results showed that the duration of irrigation 0.5 hours at intervals of 3 days, followed by the application of 15 t.ha-1 bokashi organic fertilizer could increase the bulb circle of 'Lembah Palu' varieties.The use of bokashi organic fertilizer 15 t.ha-1 could increase soil moisture so it can growth, yields, and quality of shallot bulb. The duration of irrigation with a sprinkler system for 0.5-1.0 hours at intervals of 3 days could result in the growth of total dry weight and total leaf area per plant as well as the number of tubers per clump, fresh weight of tubers per clump and yield of tubers per hectare higher than treatment of water for 1.5 hours at intervals of 3 days. Water supply regulations and the use of bokashi organic fertilizers can increase the growth, yield, and quality of LP-VoS bulbs on dryland. For the cultivation of‘Lembah Palu’ varieties of shallots in dry land, it is necessary to apply organic fertilizers to increase the soil water content for increased production and quality.


2020 ◽  
Vol 367 (20) ◽  
Author(s):  
Christoph Baum ◽  
Riya C Menezes ◽  
Aleš Svatoš ◽  
Torsten Schubert

ABSTRACT Microalgae are not able to produce cobamides (Cbas, B12 vitamers) de novo. Hence, the production of catalytically active Cba-containing methionine synthase (MetH), which is present in selected representatives, is dependent on the availability of exogenous B12 vitamers. Preferences in the utilization of exogenous Cbas equipped with either adenine or 5,6-dimethylbenzimidazole as lower base have been reported for some microalgae. Here, we investigated the utilization of norcobamides (NorCbas) for growth by the Cba-dependent Chlamydomonas reinhardtii mutant strain (ΔmetE). The growth yields in the presence of NorCbas were lower in comparison to those achieved with Cbas. NorCbas lack a methyl group in the linker moiety of the nucleotide loop. C. reinhardtii was also tested for the remodeling of NorCbas (e.g. adeninyl-norcobamide) in the presence of different benzimidazoles. Extraction of the NorCbas from C. reinhardtii, their purification, and identification confirmed the exchange of the lower base of the vitamers. However, the linker moiety of the NorCbas nucleotide loop was not exchanged. This observation strongly indicates the presence of an alternative mode of Cba deconstruction in C. reinhardtii that differs from the amidohydrolase (CbiZ)-dependent pathway described in Cba-remodeling bacteria and archaea.


2020 ◽  
Author(s):  
Arjun Chakrawal ◽  
Anke M. Herrmann ◽  
Stefano Manzoni

<p>Soil organic carbon (SOC) represents both a source of energy (catabolism) and a building material for biosynthesis (anabolism) for microorganisms. Microbial carbon use efficiency (CUE) – the ratio of C used for biosynthesis over C consumed – measures the partitioning between anabolic and catabolic processes. While most work on CUE has been based on C mass flows, the role of SOC energy content, microbial energy demand, and general energy flows on CUE have been rarely considered. Thus, a bioenergetics perspective on CUE could provide new insights on how microorganisms utilize C substrates and ultimately allow C to be stabilized in soils.</p><p>The microbial growth reactions are generally associated with a negative enthalpy change, which results in heat dissipation from the system. This heat can be measured using an isothermal calorimeter, which is often coupled with respiration measurements. This coupled system allows studying energy and C exchanges, and calculating their ratio referred to as the calorespirometric ratio (CR). Here, we formulate a coupled mass and energy balance model for microbial growth and provide a generalized relationship between CUE and CR. In the model, we consider two types of organic C in soils, the added substrate (i.e., glucose) and the native SOC. Furthermore, we assume that glucose is taken up via aerobic (AE) and two fermentation metabolic pathways – glucose to ethanol (F1) and glucose to lactic acid (F2); for simplicity, only aerobic growth on the native SOC was adopted. We use this model as a framework to generalize previous formulations and generate hypotheses on the expected variations in CR as a function of substrate type, metabolic pathways, and microbial properties (specifically CUE). In turn, the same equations can be used to estimate CUE from measured CR.</p><p>Our results show that in a non-growing system, CR depends only on the rates of different metabolic pathways (AE, F1, and F2). While in growing systems, CR is a function of rates as well as growth yields for these metabolic pathways. Under purely aerobic conditions, our model predicts that CUE increases with increasing CR when the degree of reduction of the substrate is higher than that of the microbial biomass. Similarly, CUE decreases with increasing CR when the degree of reduction of substrate is lower than that of the biomass. In the case of combined metabolism – aerobic and fermentation simultaneously – CUE is not only a function of CR and the degree of reduction of substrates but also the rates and growth yields of all metabolic pathways involved. To summarize, in this contribution we illustrate how calorespirometry can become an efficient tool to evaluate CUE and the role of different metabolic pathways in soil systems.</p>


Sign in / Sign up

Export Citation Format

Share Document