Aims The main goal of the study reported herein was to assess the nodulation performance of a Mesorhizobium strain transformed with an exogenous ACC deaminase gene (acdS), and its subsequent ability to increase chickpea plant growth under normal and waterlogged conditions. Methods The Mesorhizobium ciceri strain LMS-1 was transformed with the acdS gene of Pseudomonas putida UW4 by triparental conjugation using plasmid pRKACC. A plant growth assay was conducted to verify the plant growth promotion ability of the LMS-1 (pRKACC) transformed strain under normal and waterlogging conditions. Bacterial ACC deaminase and nitrogenase activity was measured.Results By expressing the exogenous acdS gene, the transformed strain LMS-1 showed a 127% increased ability to nodulate chickpea and a 125% promotion of the growth of chickpea compared to the wild-type strain, under normal conditions. Plants inoculated with the LMS-1 wild-type strain showed a higher nodule number under waterlogging stress than under control conditions, suggesting that waterlogging increases nodulation in chickpea. No significant relationship was found between ACC deaminase and nitrogenase activity. Conclusions The results obtained in this study show that the use of rhizobial strains with improved ACC deaminase activity might be very important for developing microbial inocula for agricultural purposes.

a b s t r a c tWe investigated whether an intact extraradical mycelium (ERM) is more effective than other forms of propagule from indigenous arbuscular mycorrhizal fungi (AMF) in providing protection against stress to a host plant. The response of wheat (Triticum aestivum L.) to Mn toxicity was studied in a two-phase greenhouse experiment. In Phase 1, four Mn tolerant species from the natural vegetation, ranging from strongly mycotrophic to non-or weakly mycotrophic, were grown to develop different amounts of ERM. Wheat was then planted (Phase 2) with the ERM fragmented by sieving (Disturbed Treatment) or kept intact with no prior soil disturbance (Undisturbed Treatment). The growth of wheat was doubled by earlier and faster mycorrhizal colonization (AC) in the presence of an intact ERM at planting. There was a positive correlation between plant growth and the reduction of Mn and enhancement of P and S uptake into shoots. However, the growth of plants in undisturbed soil was significantly affected by the ERM developer species, which was not explained by differences in AC. Colonization starting from an intact ERM greatly enhanced the potential of AMF for protection against Mn toxicity. However, the degree of protection depended on the plant previously grown to develop the ERM, suggesting that there may be functional diversity within the ERM developed by mycotrophic plants of the natural vegetation.

As functional diversity influences the benefits conferred on host plants by arbuscular mycorrhizal fungi (AMF) and large scale commercial inoculation is currently impracticable, strategies are required to manage communities of indigenous AMF associated with different hosts within agricultural cropping systems. In a non-sterilized soil, using 454 pyrosequencing of the LSU-D2 rDNA gene, host plant AMF diversity was assessed following successions of different plant species, grown with or without prior soil disturbance. Diversity present in the

Aims:  Our goal was to understand the symbiotic behaviour of a Mesorhizobium strain expressing an exogenous 1‐aminocyclopropane‐1‐carboxylate (ACC) deaminase, which was used as an inoculant of chickpea (Cicer arietinum) plants growing in soil. Methods and Results:  Mesorhizobium ciceri LMS‐1 (pRKACC) was tested for its plant growth promotion abilities on two chickpea cultivars (ELMO and CHK3226) growing in nonsterilized soil that displayed biotic and abiotic constraints to plant growth. When compared to its wild‐type form, the M. ciceri LMS‐1 (pRKACC) strain showed an increased nodulation performance of c. 125 and 180% and increased nodule weight of c. 45 and 147% in chickpea cultivars ELMO and CHK3226, respectively. Mesorhizobium ciceri LMS‐1 (pRKACC) was also able to augment the total biomass of both chickpea plant cultivars by c. 45% and to reduce chickpea root rot disease susceptibility. Conclusions:  The results obtained indicate that the production of ACC deaminase under free living conditions by Mesorhizobium strains increases the nodulation, plant growth abilities and biocontrol potential of these strains. Significance and Impact of the Study:  This is the first study regarding the use of a transformed rhizobial strain expressing an exogenous ACC deaminase in different plant cultivars growing in soil. Hence, obtaining Mesorhizobium strains with high ACC deaminase activity is a matter of extreme importance for the development of inoculants for field applications.

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