Alfalfa (Medicago sativa L.) is a crucial plant for saline and alkaline soil development, which is crucial for managing the salinization of global land resources. It can withstand saline and alkaline stress and can fix nitrogen. By secreting phytohormones, fixing nitrogen, and boosting antioxidant capacity, nitrogen–fixing bacteria, rhizobacteria, and other inter–root biotrophic bacteria encourage alfalfa development and reduce salinity stress. Alfalfa’s symbiotic association also encourages other plants to tolerate salinity and greatly boosts the amount of nitrogen in the soil. The mechanism by which inter–root growth–promoting bacteria mitigate saline and alkaline stress in alfalfa remains a prominent research focus. This paper reviews the current state of research on inter–root probiotic bacteria associated with alfalfa, utilizing literature mining to summarize the resource information of inter–root nitrogen–fixing bacteria found in saline–alkaline soils. We elucidate their nitrogen-fixing mechanisms and adaptive characteristics, explore their roles and potential applications in the improvement of saline–alkaline lands, and provide a theoretical foundation for the development of novel nitrogen–fixing bacterial fertilizers and restoration technologies for saline–alkaline environments.

Rapidly growing industrial biotechnology and bio-manufacturing require simple and cost-effective bioseparation tools. A novel strategy of bioseparation based on the streptavidin-decorated polyhydroxyalkanoate (PHA) nano-granules was developed in this study. By fusing to the N-terminus of PHA-associated phasin protein, the streptavidin was one-step immobilized on the surface of PHA nano-granules simultaneously with the accumulation of PHA in recombinant Escherichia coli. About 1.95 g/L of PHA nano-granules (54.51 wt% of cell dry weight) were produced after 48 h bacterial cultivation. The following qualitative and quantitative characterizations demonstrated that the streptavidin accounted for approximately 6.78% of the total weight of the purified PHA nano-granules and confirmed a considerable biotin affinity of 0.1 ng biotin/μg surface protein. As a proof of concept, the nano-granules were further functionalized with biotinylated oligo(dT) for mRNA isolation and about 1.26 μg of mRNA (occupied 2.59%) was purified from 48.45 μg of total RNA, achieving good integrity and high purity with few DNA and rRNA contaminations. Moreover, the nano-granules retained more than 80% of their initial mRNA recovery efficiency after ten cycles of repeated use. The PHA-SAP nano-granules were also functionalized with biotinylated magnetic beads, allowing magnetic recovery of the PHA nano-granules from cell lysates that still needs optimization. Our study provides a novel and expandable platform of PHA nano-granules that can be further functionalized with various biological groups for bioseparation applications. The functional PHA nano-granules have a great potential to serve as bioseparation resin for large-scale purification processes after suitable optimizations for “bench-to-factory” translation, contributing to scalable and sustainable bioprocessing.