Background
Increasing concern over foreign energy supplies, global greenhouse gas emissions and the need for rural economic development has driven the interest in sustainable biomass production for bioenergy and bio-products. It has been suggested that by 2025, the world energy demand will likely be increased by more than 50% 12. This demand, and societal concerns about the environmental impact of burning fossil fuels are key factors stimulating the development of national and regional strategies aimed at the growth of renewable energy supplies, primarily focused on biofuels. To reduce the reliance on fossil fuels, the USA, the world’s major energy consumer, released the Energy Independence and Security Act of 2007 that aims to increase the production of renewable fuels from 9.0 billion gallons in 2008 to 36 billion gallons by 2022 3. The recent USDA/DOE National Biofuels Action Plan 4 has helped to delineate the priority areas required to accelerate sustainable biofuel industry development. Within this document, Action Area 2 was identified as feedstock production and improvement. Various feedstocks, such as perennial rhizomatous grasses, can provide sources of lignocellulosic biomass, serving as new sources of crop growth and income for regional farmers.
One of the most promising feedstocks capable of contributing to the realization of US renewable energy goals is the common perennial grass, switchgrass (Panicum virgatum L.)5. This native prairie grass, consisting of a diverse germplasm 6, can grow on marginal lands under low inputs of water and agrochemicals 7, so that its cultivation does not compete with food crops for land and other resources. Due to its large root system and fast stand regrowth, switchgrass has other positive environmental effects, including the prevention of surface runoff and soil erosion, carbon sequestration, and the provision of a wildlife habitat 58. Switchgrass cultivated lands also had much higher total soil organic carbon deposits than lands cultivated with annual crops, such as corn and wheat 910.
The economics of biofuel production is highly dependent on feedstock cost and conversion technology 16. The development of improved switchgrass varieties for low-cost production on marginal lands is one prerequisite for the success of the bioenergy program 511. One such approach involves the use of beneficial microorganisms, such as endophytes, which form intimate associations with plants 1213. Endophytes, both fungal and bacterial, have been targeted as mechanisms to enhance plant characteristics for commercial uses 14. The colonization of grasses by fungal endophytes for performance enhancement is well documented 15, including their use with switchgrass 1617. However, to our knowledge, only one study has reported growth promotion of a bioenergy feedstock grass (Miscanthus x giganteous) seedlings by a bacterial endophyte (Herbaspirillum frisingense) 18. A key component of our bioenergy crop research program involves the utilization of beneficial bacterial endophytes that form stable and persistent associations with switchgrass, as the mechanism to improve biomass yield and enhance stress tolerance under low-input production systems 19. Beneficial bacterial endophytes are naturally occurring soil microorganisms that can penetrate plant roots and translocate to the above ground organs and, upon colonization, affect plant growth, health, and productivity 12202122. Although the molecular mechanisms of beneficial endophyte-host plant interactions are largely unknown, several studies have demonstrated that endophytes can promote plant growth by enhancing the plant’s capacity for nutrient acquisition, better water management, and/or resistance to abiotic and biotic stresses via regulation of hormones 1213142021. For instance, 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase produced by endophytes lowers the ethylene levels in host plants, reducing their response to abiotic and biotic stress, and by changing root morphology, leading to stimulation of plant growth 132324. Many known endophytes also promote plant growth by producing gibberellic acid (GA3), indole-3-acetic acid (IAA) 1825, or cytokinins 2627.
Burkholderia phytofirmans strain PsJN has been found to be a highly effective plant growth promoting bacterial endophyte, with a broad host range including potatoes, tomatoes, and grape vines 21272829303132. In addition, its genome has recently been sequenced 33, providing the genomic resources needed to develop an understanding of the mechanisms associated with this endophyte’s ability to promote plant growth. PsJN produces a high level of ACC deaminase 31, enhances host plant cold 34 and heat 35 stress tolerance, improves water management 36 and plant resistance to pathogens 3738. In this study, we report growth promotion of switchgrass cv. Alamo by Burkholderia phytofirmans strain PsJN under in vitro, growth chamber, and greenhouse conditions. To our knowledge, this is the first report detailing the switchgrass-PsJN interaction.
Results
PsJN endophytic association with switchgrass Alamo
The endophytic colonization of switchgrass by Burkholderia phytofirmans strain PsJN-GFP was visualized using confocal microscopy (Figure 1). Under the appropriate illumination, the PsJN-GFP could be clearly observed inside the roots of PsJN-inoculated plants 3 days after inoculation, while no fluorescence was observed in roots of buffer-inoculated control plants. The titer of PsJN-GFP in inoculated plants was also determined using tissue homogenates from various tissues (root, leaf and sheath) at different times (Table 1). The endophyte initially infected and colonized plant roots, and by 7 days post-inoculation, PsJN titers were still highest in the root. However, the titers increased significantly in other tissues by day 14, indicating translocation to leaves and sheaths.
<p>Figure 1 </p>Confocal images of roots taken 3 days following switchgrass cv
Confocal images of roots taken 3 days following switchgrass cv. Alamo inoculation with PsJN-GFP, showing bacterial colonization inside the roots.(A): Control and (B): PsJN- inoculated plants. (C): Control and (D): PsJN-inoculated plants. In each section (a,b,c,d), left panels were observed under fluorescent light and right panels under visible light. The bars represent 100 μm (A and B) and 20 μm (C and D).
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<p>Table 1</p>Colony-forming units (CFU) of root, leaf, and sheath tissues at different times after PsJN-GFP inoculation
Days after PsJN-
Plant tissues
Average CFU/g
|
GFP inoculation
Fresh weight
|
3
All (Roots, leaves, and sheath)
4.2X105
|
7
Roots
7.6X105
|
Leaves
2.6X103
|
14
Roots
3X104
|
Sheaths
1.3X105
|
Leaves
1.2X105
|
Effects of PsJN on Alamo growth in vitro
Young switchgrass seedlings were prepared and inoculated as described in Materials and Methods, and the non-inoculated and inoculated plants were analyzed after growth in vitro for one month. The result showed that PsJN significantly and repeatedly promoted Alamo root and shoot growth, with a 35.6% increase in shoot length, a 32.8% increase in root length, and an 83.6% increase in fresh weight, compared to the non-inoculated plants (Figure 2). After several replications, the average fresh weight of the PsJN-inoculated plants was always approximately 50% higher than non-inoculated plants.
<p>Figure 2 </p>Effects of endophyte PsJN inoculation on switchgrass cv
Effects of endophyte PsJN inoculation on switchgrass cv. Alamo growthin vitro. Data were obtained after plants were grown in incubator for 36 days. Sample number was 25, and ** means significant difference at 0.01 level between PsJN and control using student T-test.
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Effects of PsJN on Alamo growth in a growth chamber environment
As described above, PsJN significantly enhanced switchgrass cv. Alamo growth in vitro. We next assessed the impact of PsJN on growth under soil conditions. One-month-old in vitro grown Alamo (control and PsJN-inoculated seedlings) were transferred to a flat with 72 cavities filled with soil and grown in a growth chamber under 28/22°C day/night temperatures with 16 h light period for one month. The PsJN-inoculated plants showed significant growth increases compared to control plants in shoot length and fresh/dry weights (Figure 3). The growth chamber experiments were repeated 5 times, and the average data from 5 experiments showed significant growth promotion by PsJN, with a 46.3%, and a 54.1% increase in fresh weight and dry weight, respectively. The total dry weight increase (54.1%) by PsJN was more than the total fresh weight increase (46.3%), indicating that the PsJN-inoculated plants accumulated more biomass.
<p>Figure 3 </p>Effects of endophyte PsJN inoculation on switchgrass cv
Effects of endophyte PsJN inoculation on switchgrass cv. Alamo growth in growth chamber. The seedlings were inoculated with PsJN and grown in vitro for one month, then transferred to soil and grown in growth chamber for another month. Dry weight was determined after samples were dried in oven at 65°C for one day. Sample number was 36, and ** means significant difference at 0.01 level between PsJN and control using student T-test.
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Effects of PsJN on Alamo growth in the greenhouse
Non-inoculated and PsJN-inoculated plants were also grown under greenhouse conditions to determine growth enhancement persistence. The plants inoculated with PsJN and grown in vitro for 25 days were transferred to 4-gallon pots with 5 plants in each pot and grown in the greenhouse. The plants inoculated with PsJN exhibited sustained growth vigor, as they were significantly taller, and more tillers developed early compared with the non-inoculated control plants (Figure 4). Following one month of growth in the greenhouse, the PsJN-inoculated plants had 76.2% more tillers than the control plants. The plants were harvested following growth for two months, and the biomass yield determined (Figure 5). The PsJN-inoculated plants were repeatedly significantly higher in biomass yield, with a 36.8% increase in fresh weight and a 57.1% increase in dry weight.
<p>Figure 4 </p>Plant growth and tiller development after control and PsJN inoculated plants were transferred to 4-gallon pots and grown in greenhouse
Plant growth and tiller development after control and PsJN inoculated plants were transferred to 4-gallon pots and grown in greenhouse.
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<p>Figure 5 </p>Growth promotion persistence of Alamo in greenhouse by PsJN inoculation
Growth promotion persistence of Alamo in greenhouse by PsJN inoculation. The seedlings were inoculated with PsJN and grown in vitro for one month, then transferred to 4-gallon pot with 5 plants/pot and grown in greenhouse for two months. Dry weight was determined after samples were dried in oven at 65°C for one day. Sample number was 25, and ** means significant difference at 0.01 level between PsJN and control using student T-test.
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Effects of PsJN on Alamo growth in sub-optimal conditions
In order to develop a low input and sustainable switchgrass feedstock production system utilizing the beneficial bacterial endophyte, we tested growth performance of PsJN-inoculated plant with unfertilized field soil, in a glasshouse under ambient conditions during the Fall, when the temperature was not optimal for switchgrass growth. The results showed that PsJN-inoculated plants produced twice the total biomass of controls (Figure 6).
<p>Figure 6 </p>Growth promotion of Alamo by PsJN inoculation in sub-optimal conditions
Growth promotion of Alamo by PsJN inoculation in sub-optimal conditions. The seedlings were inoculated with PsJN and grown in vitro for one month, then transferred to 4-gallon pots with 5 plants/pot with unfertilized field soil and grown in the glasshouse under ambient conditions for 2.5 months in the late Fall of 2010. Dry weight was determined after samples were dried in oven at 65°C for one day. Sample number was 25, and ** means significant difference at 0.01 level between PsJN and control using student T-test.
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Direct inoculation of switchgrass seeds with PsJN
In order to explore a practical way to inoculate switchgrass with the bacterial endophyte, we sterilized switchgrass seeds as described in Materials and Methods, placed the sterilized seeds on wet filter paper for 3-5 days in an incubator at 25°C, and then inoculated the germinating seeds with different concentrations of endophyte inoculum to determine the optimal inoculation concentration (OD600 at 0.1-0.5). The plants inoculated with PsJN at OD600 of 0.1, 0.25, and 0.5 exhibited 28.7%, 55.0% and 80.1% increases in dry weight, respectively, compared to non-inoculated plants after grown in vitro for 25 days and in growth chamber for another month. A PsJN concentration of 0.5 was the most effective at promoting biomass increase (Figure 7), and no biomass difference was observed between the 0.1 treatment and control.
<p>Figure 7 </p>Effects of different concentrations of PsJN on swtchgrass cv
Effects of different concentrations of PsJN on swtchgrass cv. Alamo growth with direct seed inoculation. The surface-sterilized seeds were infected with different concentrations of PsJN and grown in vitro for 17 days, then transferred to 72-cavity trays and grown in a growth chamber for 50 days. * and ** mean significant difference at 0.05 and 0.01 levels respectively between PsJN and control using student T-test.
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Endophyte infection and colonization of seeds are dependent on endophyte concentration and the status of seed imbibitions. So, in order to facilitate infection and colonization by the bacterial endophyte, the sterilized seeds were imbibed in water for 1, 2, 3, or 4 days, and then inoculated with PsJN at an OD600 of 0.5 or 1.0, since an OD600 of 0.5 was the most effective as described above. The PsJN-inoculated seeds were placed in an incubator at 25°C with a 16 h light period for 25 days, and transferred to soil and grown in a growth chamber for 37 days. The results indicated that plants from the seeds imbibed for 2 days and then inoculated with an OD600 of 0.5 had the highest dry weight, with a 55% increase compared to non-inoculated control plants (Figure 8).
<p>Figure 8 </p>Effects of different concentrations of PsJN on switchgrass cv
Effects of different concentrations of PsJN on switchgrass cv. Alamo growth with direct inoculation of seeds that were imbibed in water for different days (1-4 days). The seeds were infected with different concentrations of PsJN and grown in vitro for 25 days, then transferred to 72-cavity trays and grown in a growth chamber for 37 days. Sample number was 72 for each treatment. * and ** mean significant difference at 0.05 and 0.01 levels respectively between PsJN and control using student T-test.
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Genotypic responses to PsJN
As described above, PsJN was able to stimulate growth in switchgrass cv. Alamo. To assess the influence of plant genotype on this response, seven other switchgrass cultivars were tested for their growth responses to PsJN. As shown in Table 2, growth promotion by PsJN was genotype-dependent. The switchgrass cvs. Forestburg, Nebraska, and Blackwell were all responsive to PsJN, with measured significant growth increases of 60.1%, 26.8%, and 23.0%, respectively, while the cvs. Cave-in-Rock, Sunburst, Shelton, and Shawnee did not exhibit growth promotion in response to PsJN under similar conditions. Preliminary result from Cave-in-Rock bioassay indicated that PsJN titers were not sustained after inoculation and were much lower in the non-responsive plants following inoculation.
<p>Table 2</p>Effects of B. phytofirmans PsJN on plant growth in different switchgrass cultivars
Cultivars
Treatment
No. plants
Root length (cm)
Shoot length (cm)
Total fresh weight (mg)
PsJN/control (%)a
|
a PsJN/control (%) means total fresh weight of PsJN inoculated plants over that of control plants.
b p-value means degrees of statistical significance between PsJN treatment and control using student T-test.
Shawnee
Control
24
2.3
8.4
50.1
|
PsJN
24
2.1
7.8
58.8
117.4
|
p-valueb
0.2037
0.2049
0.0717
|
Nebraska
Control
24
1.5
10.3
40.9
|
PsJN
24
1.5
11.6
51.9
126.8
|
p-value
0.4160
0.0656
0.0055
|
Forestburg
Control
34
1.6
8.6
33.7
|
PsJN
30
1.8
12.7
54.0
160.1
|
p-value
0.1986
0.0000002
0.0000001
|
Shelton
Control
28
3.3
14.1
117.7
|
PsJN
28
3.0
12.0
135.3
115.0
|
p-value
0.1579
0.0067
0.0907
|
Blackwell
Control
28
1.4
9.9
52.6
|
PsJN
28
1.5
11.3
64.7
123.0
|
p-value
0.2970
0.0998
0.0543
|
Sunburst
Control
30
0.8
8.5
33.0
|
PsJN
28
0.9
10.4
26.4
80.0
|
p-value
0.2985
0.0137
0.0731
|
Cave-in-Rock
Control
33
2.8
14.7
107.8
|
PsJN
34
3.1
13.8
113.4
105.2
|
p-value
0.2317
0.4052
0.5613
|
Discussion
In the present study, we demonstrated the ability of B. phytofirmans PsJN to colonize and promote growth in switchgrass cv. Alamo. Three days following PsJN inoculation, we could clearly visualize bacterial colonization inside the roots under confocal microscopy. The bacterial population inside the roots was initially much higher than that of the leaves and sheaths, and the bacterial endophyte was subsequently translocated vertically to the upper leaves through the leaf sheath. These results were similar to that reported for grapevine 22 and potato 39, where PsJN was transported through the interior vascular system, from root xylem vessels to the upper parts of the plants. This is a critical first step in the endophytic bacteria-plant interaction 40. We observed significant growth promotion of cv. Alamo by PsJN, under both in vitro and soil conditions. Our study showed total fresh weight and total dry weight of the inoculated plants was increased by 45% and 55% respectively compared with the non-inoculated control plants when the inoculated seedlings were grown in vitro and then transferred to soil and grown in growth chamber for one month. Similar results have been obtained in 4-gallon pots under our greenhouse conditions. Other studies have reported levels of growth promotion by PsJN, with grapevine showing a 6-fold increase in total biomass 34, and potato showing an approximate 2-fold increase in root and haulm biomass 36 over controls. The mechanism of plant growth by B. phytofirmans PsJN has been reported 21 and attributed to the ability of PsJN to produce high levels of ACC deaminase activity, which degrades ACC to ammonia and α-ketobutyrate 41, which is a common characteristic of plant growth promoting bacteria. ACC is the precursor to ethylene, a plant stress hormone; hence, the reduced ethylene level in PsJN-colonized plants will promote plant growth. According to the report by Penrose and Glick (2003) 42, ACC activity over 20 nmol α-ketobutyrate/h/mg is sufficient to promote host plant growth, and PsJN has been shown to contain 308 nmol α-ketobutyrate/h/mg of ACC deaminase activity 31. Although several studies have reported the interaction between this endophyte and host plants for growth promotion, most studies have reported in vitro data 22272836. Our results with unfertilized field soil, in a glasshouse under ambient conditions during the Fall, when the temperature was not optimal for switchgrass growth (Figure 6) implied the potential benefit of switchgrass inoculated with PsJN for growth on marginal lands and sub-optimal growth conditions. Although our results indicate potential benefit of bacterial endophytes in switchgrass under in vitro, growth chamber and greenhouse conditions, much work still needs to be done in assessing growth promotion of switchgrass by endophytes in the field since there is much more competition between endophytes and other microorganisms in addition to many other unfavorable conditions. While our initial studies were carried out with cv. Alamo, we tested the utility of PsJN as a growth-promoting endophyte with other switchgrass cultivars. Our results indicated that specific genotype effects existed, with some genotypes being highly responsive to the growth promotive effects of PsJN, and others not. Similar genotype effects have been reported by others. It was reported that the potato response to PsJN involves some form of genetic control, as some potato cultivars display the beneficial response to the endophyte, while others do not 354344. The typical in vitro phenotype for a strongly responsive cultivar was characterized by a massive, well-branched root system and after the first 3-4 weeks in culture, the plantlet was developmentally more advanced than the non-bacterized controls. Stems were sturdier, with more lignin deposits around the vascular system, and the plantlets developed more root hairs and more and larger leaf trichomes 43. We also noticed PsJN-inoculated switchgrass plants were developmentally advanced (unpublished data). Such enhancements were not apparent for the poorly-responsive cultivars. We also observed some of these phenotypic differences between PsJN-responsive and non-responsive switchgrass cultivars. Additional work illustrating the genetic control of the beneficial response to the endophyte used monoploid potato lines derived from anther culture of an adapted diploid Solanum phureja clone, BARD 1-3 44. The diploid anther donor, BARD 1-3, exhibited a bacterization response comparable to Red Pontiac, while monoploid lines exhibited a response to PsJN ranging from favorable to unfavorable to neutral. The assumption here was that the response range of the monoploid population was due to the segregation of alleles for genes involved in regulating the positive or negative interaction with PsJN.
The potato/PsJN studies have been the most characterized, and carried out with material clonally propagated via nodal sections, in which a single inoculation is sufficient to initiate colonization through the xylem tissue, eventually spreading to the upper leaves 36. Bacterial levels must reach a threshold population within the plant before they are effective 45 with a direct relationship between plantlet growth enhancement and PsJN colonization of both interior and exterior surfaces 44. The PsJN colonization profiles for a responsive and poorly responsive cultivar over 8 tissue culture generations revealed bacterial loads one order of magnitude greater for shoot/root surface and interior colonization in the responsive compared to the poorly responsive cultivar. Furthermore, the responsive cultivar exhibited increased colonization over successive generations, while the poorly responsive cultivar exhibited declining bacterial populations over successive generations. We are currently assessing the level of colonization in switchgrass cultivars responsive and non-responsive to PsJN to determine the degree of similarity between switchgrass and potato responses to the endophyte. At present, the mechanisms governing B. phytofirmans PsJN genotype-specificity in growth promotion of switchgrass (and other plants) are unknown, although we are currently using large scale gene expression analyses to determine the differences in the switchgrass molecular responses between differently-responding cultivars. In summary, the results reported here illustrate the ability of B. phytofirmans PsJN to infect and colonize responsive switchgrass (Panicum virgatum) cultivars like Alamo, and to promote plant growth. This study lays the foundation to develop a low input and sustainable switchgrass feedstock production system on marginal lands using this, and other, beneficial bacterial endophytes.
Methods
Plant materials
Switchgrass (Panicum virgatum L.) cvs. Alamo and Cave-in-Rock seeds were purchased from Warner Brothers Seed Co. (Lawton, OK), and other switchgrass seeds were kindly provided by Dr. Bingyu Zhao (Department of Horticulture - Virginia Tech, Blacksburg, VA). Switchgrass seeds were surface-sterilized by treatment with 70% ethanol for 2 min, rinsed 3X with distilled water, de-husked for 30 min with 60% H2SO4 with stirring, washed 3X with distilled water, sterilized with 0.4 M sodium hypochlorite (50% commercial bleach solution containing 6% sodium hypochlorite) containing 0.1% Triton 100 for 30 min followed by 5X rinse with sterile, deionized, distilled water (ddH2O).
Bacterial endophyte and culture conditions
Burkholderia phytofirmans strain PsJN 31 and its PsJN-GFP derivative 22 were obtained from Dr. Angela Sessitsch (Austrian Institute of Technology, Seibersdorf, Austria). The cultures were streaked on King’s B (KB) solid medium as described in 45. Inoculum was produced by transferring one loop of PsJN from 2-day-old cultures to 5 ml KB broth in a 15-ml culture tube, followed by incubation at 28°C on a shaker (150 rpm) overnight. Five ml of the overnight PsJN culture was added to 45 ml KB broth in a 250-ml Erlenmeyer flask and grown to 0.7 OD600. Bacterial cells were then collected by centrifugation at 3,500 rpm for 7 min at 4°C, and re-suspended in PBS buffer (10 mM NaH2PO4 containing 0.8% NaC1, pH 6.5) after which the OD600 was adjusted with PBS buffer to 0.5, unless described otherwise.
Seedling inoculation with PsJN and plant growth responses
Surface-sterilized seeds were germinated in petri-dishes for 7 days at 25°C, under white fluorescent light (67 μmol m-2 s-1), 16 h photoperiod, on a switchgrass growth medium consisting of MS salts and vitamins 46, 30 g/l maltose and 3 g/l phytogel, pH 5.8. The root tips of the young seedlings were cut prior to PsJN inoculation to facilitate bacterial penetration 45. For the direct seed inoculation surface-sterilized seeds were placed on wet filter paper for 3-5 days in an incubator at 25°C with 16 h photoperiod (white fluorescent bulbs at 67 μmol m-2 s-1) followed by soaking in PsJN solution (0.5 of OD600) for 1 min. Control seedlings/seeds were treated with PBS buffer alone. The treated seedling/seeds were blot-dried with sterile paper towel, placed on switchgrass growth medium in GA7 Magenta vessels (Sigma-Aldrich) containing 50 ml of media and 5 seedlings or germinating seeds per vessel, and grown for one month in the incubator as above. Root and shoot length, and seedling fresh weight were then determined, and the plants transferred to a soil mix composed of 2/3 Miracle-Gro® Potting Mix (Scotts Miracle-Gro Company, Marysville, Ohio) and 1/3 Arabidopsis growing media (Lehle Seeds, Round Rock, Texas). Plants were grown in 72-cavity trays in a growth chamber at a 28/22°C day/night temperature, 16 h photoperiod (white fluorescent bulbs at 88 μmol m-2 s-1) for 30 days, or 4-gallon pots in the greenhouse.
PsJN colonization
The plants inoculated with PsJN-GFP were examined under a fluorescent stereomicroscope (Model SZX-ILLD2-100; Olympus, Tokyo, Japan) equipped with a GFP filter (BP460-490, Olympus, Tokyo, Japan) and the Zeiss 510 laser scanning confocal microscope (LSCM) (Carl Zeiss, Inc., Thornwood, NY) to observe colonization.
For bioassays, the control and PsJN-GFP inoculated plants were surface-sterilized with 0.032 M sodium hypochlorite for 1 min, then washed 4X with sterile distilled water. Fifty μl of the final wash was plated on solid KB medium to confirm effectiveness of surface sterilization. Root, leaf and sheath parts were then separated, each weighed, and ground with mortar and pestle in 1 ml sterile distilled water. The homogenates were then centrifuged at 2000 rpm for 3 min, and the supernatant diluted to 1:10, 1:100, and 1:1000 with distilled water. Fifty μl samples of the serially diluted solutions were spread on solid KB medium. The plates were incubated for 3 days at 28°C in the dark and the number of GFP-positive colonies determined using fluorescence stereomicroscopy as described above.