Nutritional Requirement for the Expression of Nitrogenase Activity by Rhizobium sp. in Agar Culture

The effect of various carbon sources, nitrogen sources, vitamins and trace elements on the ability of three strains (32H1, CB627, CB744) of a slow-growing Rhizobium sp. to develop nitrogenase activity in agar culture was studied. Strains 32H1 and CB627 developed nitrogenase but showed differences with respect to the nature and concentrations of carbon sources required for optimum activity. Strain 32H1 had less specific requirements than CB627 in this respect and could sustain high nitrogenase activity over a wider range of phosphate concentration (5 to 60 mmol/1) in the medium than CB627. There were only minor differences between these two strains with respect to the nitrogen source [glutamine, asparagine, histidine or (NH₄SO₄] required in the medium for nitrogenase induction, and nitrogenase activity in both strains was unaffected by changes in the concentration of vitamins or trace elements supplied. Strain CB744 did not develop nitrogenase activity under any of the conditions tested. Adenosine 3', 5'-cyclic monophosphate (1 mmol/1) was found to accelerate derepression of nitrogenase synthesis in agar cultures of strains 32H1 and CB627.     

EXPERIMENTS ON THE ACCURACY OF SURFACE DROP BACTERIAL COUNTS

SUMMARY: A statistical experiment has shown that no significant proportion of the errors of determination of bacterial populations by the surface drop method could be attributed to the dropping technique employed. With both pure and mixed cultures the numbers of colonies/drop followed a Poisson distribution very closely.
It is suggested that in order to determine bacterial populations at a consistent level of accuracy a constant number of colonies should be counted rather than a constant number of drops. Whenever it is justified, the confidence limits for the results of counts should be quoted.     

Effectiveness of Lotus Root Nodules: III. EFFECT OF COMBINED NITROGEN ON NODULE EFFECTIVENESS AND FLAVOLAN SYNTHESIS IN PLANT ROOTS

When grown in a nutrient solution containing combined nitrogen(NH₄NO₃), Lotus pedunculatus and L. tenuis seedlings inoculatedwith a fast-growing strain of Rhizoblum (NZP2037) did neitherdevelop root nodules nor develop flavolans in their roots. Incontrast, the roots of nodulated seedlings growing in a nitrogen-freenutrient solution contained flavolans. Flavolan synthesis coincidedwith root nodule development on these plants. When added as a single dose, high concentrations of NH₄NO₃ (5and 10 mg N per plant) stimulated the growth of L. pedunculatusplants but suppressed nodulation and nitrogen fixation. In contrastthe continued supply of a low concentration of NH₄NO₃ (1?0 mgN d^–1 per plant) stimulated nitrogen fixation by up to500%. This large increase in nitrogen fixation was associatedwith a large increase in nodule fresh weight per plant, a doublingof nodule nitrogenase activity, and a lowering of the flavolancontent of the plant roots. The close relationship between nitrogendeficiency, nodule development, and flavolan synthesis in L.pedunculatus meant that it was not possible (by nitrogen pretreatmentof plants) to alter the ineffective nodule response of a Rhizobiumstrain (NZP2213) sensitive to the flavolan present in the rootsof this plant.     

Effectiveness of Lotus Root Nodules: I. MORPHOLOGY AND FLAVOLAN CONTENT OF NODULES FORMED ON LOTUS PEDUNCULATUS BY FAST-GROWING LOTUS RHIZOBIA

The morphology of root nodules formed on Lotus pedunculatusby two fast-growing strains of Rhizobium, NZP2037 which formseffective (nitrogen-fixing) nodules and NZP2213 which formsineffective (non-nitrogen-fixing) nodules, has been studied.The nodules formed by NZP2037 contained a central zone of bacteroid-filledplant cells surrounded by a cortex. In contrast the nodulesformed by NZP2213 contained no Rhizoblum-infected plant cells,but rhizobia were found in localized areas on the nodule surfaceand between the outer two or three cell layers of the nodule.Electron-dense osmiophilic deposits identified as flavolans(condensed tannins) were present in the vacuoles of many uninfectedplant cells in the nodules formed by both Rhizobium strains.This is the first time that flavolans have been positively identifiedin legume root nodules. In the NZP2037 nodule flavolans werepresent in the outer cortical and epidermal cells. In the ineffecitveNZP2213 nodule fiavolans were present in many of the centralnodule cells. The concentration of flavolan in the NZP2213 nodulewas 12 times higher than in the NZP2037 nodule.     

Effectiveness of Lotus Root Nodules: II. RELATIONSHIP BETWEEN ROOT NODULE EFFECTIVENESS AND 'IN VITRO' SENSITIVITY OF FAST-GROWING LOTUS RHIZOBIA TO FLAVOLANS

An extract from the roots of Lotus pedunculatus plants was foundto contain a compound toxic towards fast-growing Lotus rhizobia.This compound was identified as a flavolan, which has a prodeiphinidin:procyanidin ratio of 75:25. A fast-growing strain of Rhizobium(NZP2213) which forms ineffective root nodules on L. pedunculatuswas four times more sensitive to this flavolan (ED₅₀ = 25 ?gml^–1) than another strain (NZP2037, ED₅₀ = 100 ?g ml^–1)which forms effective root nodules on this species. The rootsof another Lotus species, L. tenuis, on which both strains ofRhizobium form effective root nodules, also contained a flavolan( 95% procyanidin) but both strains were relatively insensitiveto this flavolan (EDED₅₀ = 350 to 500 ?g ml^–1) L. pedunculatusplants bearing ineffective root nodules contained two to threetimes more flavolan in their roots (5–7 mg g^–1 fr.wt.)than uninoculated control plants. Experiments with seven otherLotus species and with hybrid plants developed between L. pedunculatusand L. tenuis showed a relationship between the prodeiphinidin:procyanidin ratio of the flavolan in their roots and the effectivenessof root nodules formed on these plants by NZP2213. Quantitativebinding studies of the flavolan from L. pedunculatus to NZP2037and NZP2213 indicated that, while the affinity constants forbinding were similar for both strains, the surface of strainNZP2037 contained four times more binding sites than NZP2213,possibly correlating with this strain's ability to toleratehigher concentrations of this flavolan. It is suggested thatthe differential sensitivity of these two strains of Rhizobiumto flavolans is related to their ability to form effective rootnodules on Lotus species.     

Effects of Water Stress on the Respiratory and Nitrogen-fixing Activity of Soybean Root Nodules

Seventy-five per cent of the N₂-fixing activity (measured asthe reduction of C₂H₂ to C₂H₄) and 50 per cent of the respiratoryactivity of detached soybean root nodules was lost when thewater potential () of the nodules was lowered from approximately–1 ? 105 Pa (turgid nodules) to –9 ? 105 Pa (moderatelystressed nodules). Severely stressed nodules ( = –1.8? 10⁶ Pa) showed almost total loss of N₂-fixing activity andup to 80 per cent loss of respiratory activity. Increasing theoxygen partial pressure (PO₂) from 10⁴ to 10⁵ Pa completelyrestored both N₂-fixation and respiration in moderately stressednodules, but only partial recovery was possible in severelystressed nodules. The activity of the stressed nodules was verylow at low PO₂ (5 ? 10³ and 10⁴ Pa). The C₂H₂-reducing activityof nodule slices, nodule breis, and bacteroids from turgid andmoderately stressed nodules was almost identical but some activitywas lost in the breis and bacteroids from severely stressednodules. Calculations showed that at low PO₂ (10⁴ and 2 ? 10⁴Pa), the rate of O₂ diffusion into severely stressed noduleswas ten times lower than that for turgid nodules, but only fourtimes lower at a higher PO₂ (4 ? 10⁴ Pa). Carbon monoxide inhibitionof C₂H₂ reduction was slower in stressed nodules than in turgidnodules. The results are discussed in view of the possible developmentof a physical barrier to gaseous diffusion and/or the possiblealtered affinity of the nodule leghaemoglobin for O₂ in thewater-stressed nodules.     

THE BIOLOGICAL OXIDATION OF SPENT GAS LIQUOR

SUMMARY: Mixed cultures of bacteria grown in spent gas liquor readily oxidized phenol, o -, m - and p -cresol, catechol, 3-methyl catechol, 4-methyl catechol, resorcinol, 2-methyl resorcinol, and 4-methyl resorcinol. Quinol, pyrogallol and phloroglucinol were more resistant. The optimum temperature was 30° and the best pH range 6·5–7·8. Yeast extract and sterile sewage sludge both increased the rate of growth of organisms in liquor when the inoculum was small. Five phenol oxidizing organisms were isolated in pure culture. Copper in concentrations greater than 1 p/m inhibited both growth and phenol oxidation by one of these.
Mixed cultures grown in an ammonium thiocyanate medium originally inoculated with Thiobacillus thiocyanoxidans oxidized potassium thiocyanate and sodium thiosulphate. Chloride inhibited thiocyanate oxidation in concentrations above 5,000 p/m, although adaptation to 15,000 p/m was possible. Phenol inhibited thiocyanate oxidation in concentrations of 300 p/m or more. Mixed cultures grown on sodium thiosulphate oxidized sodium trithionate and tetrathionate, potassium pentathionate and hexa-thionate, and potassium and ammonium thiocyanate
Manometric determinations of the 5 day biological oxygen demand of effluents after treatment showed good agreement with the values obtained by the conventional method, the manometric values being usually somewhat higher.